Correction to: Genetics in Medicine 2021; https://doi.org/10.1038/s41436-021-01232-8; published online 23 June 2021
In the prior version of this article the author name Geoffrey S. Pitt was incorrectly written as Geoffrey Pitt. The original article has been corrected.
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Authors and Affiliations
Division of Genetics and Genomics, Department of Pediatrics, Boston Children’s Hospital, Boston, MA, USA
Lance H. Rodan & Emily O’Heir
Department of Neurology, Boston Children’s Hospital, Boston, MA, USA
Lance H. Rodan
Division of Medical Genetics, Department of Pediatrics, Duke Health, Durham, NC, USA
Rebecca C. Spillmann & Vandana Shashi
Department of Pharmacology, Alberta Diabetes Institute, University of Alberta, Edmonton, AB, Canada
Harley T. Kurata, Shawn M. Lamothe & Jasmine Maghera
Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany
Rami Abou Jamra, Chiara Kloeckner & Konrad Platzer
Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA
Anna Alkelai
Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland
Stylianos E. Antonarakis, Xavier Blanc & Emmanuelle Ranza
Division of Genetic Medicine, Lausanne University Hospital, Lausanne, Switzerland
Isis Atallah
Pediatric Neurology Unit, Edmond and Lily Safra Children’s Hospital, Sheba Medical Center, Tel-Hahsomer, Israel
Omer Bar-Yosef
Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel
Omer Bar-Yosef, Yoav Bolkier, Aviva Eliyahu & Ben Pode-Shakked
CHU de Poitiers, Service de Génétique, EA3808 NEUVACOD, Poitiers, France
Frédéric Bilan
Department of Medical Genetics, Oslo University Hospital, Oslo, Norway
Kathrine Bjorgo
CHU d’Angers, Service de Pédiatrie, EA3808 NEUVACOD, Angers, France
Patrick Van Bogaert
Pediatric Cardiology Unit, Edmond and Lily Safra Children’s Hospital, Sheba Medical Center, Tel-Hahsomer, Israel
Yoav Bolkier
Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA
Lindsay C. Burrage, Lisa Emrick & Jill A. Rosenfeld
Department of Paediatrics and Child Health, Red Cross War Memorial Children’s Hospital, University of Cape Town, Cape Town, SA, South Africa
Björn U. Christ & Kirsten A. Donald
Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine in St. Louis, St. Louis, MO, USA
Jorge L. Granadillo, Patricia Dickson & Rachel Slaugh
Service de Génétique Moléculaire et Génomique, CHU, Rennes, France
Christèle Dubourg
University of Rennes, CNRS, IGDR, UMR 6290, Rennes, France
Christèle Dubourg
The Danek Gertner Insitute of Human Genetics, Sheba Medical Center, Tel-Hahsomer, Israel
Aviva Eliyahu
Edmond and Lily Safra Children’s Hospital, Sheba Medical Center, Tel-Hahsomer, Israel
Aviva Eliyahu
Center for Pediatric Genomic Medicine, Children’s Mercy Hospital, Kansas City, MO, USA
Kendra Engleman & Isabelle Thiffault
Rare Diseases and Medical Genetic Unit, IRCCS Bambino Gesù Children’s Hospital, Rome, Italy
Michaela Veronika Gonfiantini & Marina Macchiaiolo
Pediatric Neurology, Lausanne University Hospital, Lausanne, Switzerland
Jean-Marc Good, Judith Kalser, Eliane Roulet-Perez & Andrea Superti-Furga
Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands
Guus Lachmeijer & Richard H. van Jaabrsveld
Unit of Neuromuscular and Neurodegenerative Diseases, Department of Neurosciences and Neurorehabilitation, IRCCS Bambino Gesù Children’s Hospital, Rome, Italy
Francesco Nicita
Service de Génétique Clinique, Centre de référence “Maladies Rares” Anomalies du développement CLAD-Ouest, Hôpital SUD, Échirolles, France
Sylvie Odent
Center for Mendelian Genomics and Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA
Emily O’Heir
Division of Neurology, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
Xilma Ortiz-Gonzalez
Instituto de Genética Médica y Molecular (INGEMM), Hospital Universitario La Paz, IdiPAZ, CIBERER, ISCIII, Madrid, Spain
Marta Pacio-Miguez, María Palomares-Bralo & Fernando Santos-Simarro
Cincinnati Children’s Hospital and Medical Center Cincinnati, Cincinnati, OH, USA
Loren Pena
University of Cincinnati College of Medicine Cincinnati, Cincinnati, OH, USA
Loren Pena
Institute of Molecular and Clinical Ophthalmology Basel (IOB), Basel, Switzerland
Mathieu Quinodoz
Department of Ophthalmology, University of Basel, Basel, Switzerland
Mathieu Quinodoz
Division of Genomic Diagnostics, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
Avni Santani
Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA
Avni Santani & Cara Skraban
Institute of Rare Diseases, Edmond and Lily Safra Children’s Hospital, Sheba Medical Center, Tel-Hahsomer, Israel
Ben Pode-Shakked
Division of Human Genetics, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
Cara Skraban
Service de Génétique Médicale, CHU Nantes, France; Inserm, CNRS, Univ Nantes, l’institut du thorax, Nantes, France
Marie Vincent
Cardiovascular Research Institute, Weill Cornell Medicine, New York, NY, USA
Hong-Gang Wang & Geoffrey S. Pitt
The Saxon Epilepsy Center Kleinwachau, Radeberg, Germany
Pia Zacher
The Children’s Mercy Hospital, Kansas City, MO, USA
Eric Rush
Department of Pediatrics University of Missouri—Kansas City, Kansas City, MO, USA
Eric Rush
Department of Internal Medicine, University of Kansas Medical Center, Kansas City, MO, USA
Eric Rush
Alberta Children’s Hospital Research Institute, Department of Genetics, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada
Ping Yee Billie Au
BCM Clinical, Houston, TX, USA
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Mayo Clinic, Rochester, MN, USA
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Miami, Miami, FL, USA
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NIH, Bethesda, MD, USA
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NIH UDP, DRM, Bethesda, MD, USA
Eva Baker
NIH UDP, NHGRI, Bethesda, MD, USA
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Stanford, Stanford, CA, USA
Euan A. Ashley, Gill Bejerano, Jonathan A. Bernstein, Devon Bonner, Terra R. Coakley, Liliana Fernandez, Paul G. Fisher, Laure Fresard, Jason Hom, Yong Huang, Jennefer N. Kohler, Elijah Kravets, Marta M. Majcherska, Beth A. Martin, Shruti Marwaha, Colleen E. McCormack, Archana N. Raja, Chloe M. Reuter, Maura Ruzhnikov, Jacinda B. Sampson, Kevin S. Smith, Shirley Sutton, Holly K. Tabor, Brianna M. Tucker, Matthew T. Wheeler, Diane B. Zastrow & Chunli Zhao
UAB CC, Birmingham, AL, USA
William E. Byrd, Andrew B. Crouse, Matthew Might, Mariko Nakano-Okuno & Jordan Whitlock
UCLA, Los Angeles, CA, USA
Gabrielle Brown, Manish J. Butte, Esteban C. Dell’Angelica, Naghmeh Dorrani, Emilie D. Douine, Brent L. Fogel, Irma Gutierrez, Alden Huang, Deborah Krakow, Hane Lee, Sandra K. Loo, Bryan C. Mak, Martin G. Martin, Julian A. Martínez-Agosto, Elisabeth McGee, Stanley F. Nelson, Shirley Nieves-Rodriguez, Christina G. S. Palmer, Jeanette C. Papp, Neil H. Parker, Genecee Renteria, Rebecca H. Signer, Janet S. Sinsheimer, Jijun Wan, Lee-kai Wang, Katherine Wesseling Perry & Jeremy D. Woods
University of Utah, Salt Lake City, UT, USA
Justin Alvey, Ashley Andrews, Jim Bale, John Bohnsack, Lorenzo Botto, John Carey, Laura Pace, Nicola Longo, Gabor Marth, Paolo Moretti, Aaron Quinlan, Matt Velinder & Dave Viskochil
University of Utah/ARUP, Salt Lake City, UT, USA
Pinar Bayrak-Toydemir & Rong Mao
UO MOSC, Eugene, OR, USA
Monte Westerfield
Vanderbilt, Nashville, TN, USA
Anna Bican, Elly Brokamp, Laura Duncan, Rizwan Hamid, Jennifer Kennedy, Mary Kozuira, John H. Newman, John A. PhillipsIII, Lynette Rives, Amy K. Robertson, Emily Solem & Joy D. Cogan
Washington University Clinical, St. Louis, MO, USA
F. Sessions Cole, Nichole Hayes, Dana Kiley, Kathy Sisco, Jennifer Wambach, Daniel Wegner, Dustin Baldridge, Stephen Pak, Timothy Schedl, Jimann Shin & Lilianna Solnica-Krezel
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Correspondence to Vandana Shashi.
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Rodan, L.H., Spillmann, R.C., Kurata, H.T. et al. Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations. Genet Med 23, 2016 (2021). https://doi.org/10.1038/s41436-021-01306-7
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DOI: https://doi.org/10.1038/s41436-021-01306-7
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