Daliya Kancheva MSc, Derek Atkinson MSc, Peter De Rijk PhD, Magdalena Zimon PhD, Teodora Chamova MD, PhD, Vanyo Mitev MD, DSc, Ahmet Yaramis MD, Gian Maria Fabrizi MD, PhD, Haluk Topaloglu MD, PhD, Ivailo Tournev MD, DSc, Yesim Parma MD, PhD, Esra Battaloglu PhD, Alejandro Estrada-Cuzcano PhD and Albena Jordanova PhD
Genet Med advance online publication, October 22, 2015; doi:10.1038/gim.2015.139
In the published version of this article, Dr. Yesim Parman’s name was misspelled. The publisher regrets the error.
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The online version of the original article can be found at 10.1038/gim.2015.139
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Erratum: Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencing. Genet Med 18, 108 (2016). https://doi.org/10.1038/gim.2015.174
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DOI: https://doi.org/10.1038/gim.2015.174
