Showing 1–7 of 7 results
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Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss
- Christopher J Klein
- , Maria-Victoria Botuyan
- , Yanhong Wu
- , Christopher J Ward
- , Garth A Nicholson
- , Simon Hammans
- , Kaori Hojo
- , Hiromitch Yamanishi
- , Adam R Karpf
- , Douglas C Wallace
- , Mariella Simon
- , Cecilie Lander
- , Lisa A Boardman
- , Julie M Cunningham
- , Glenn E Smith
- , William J Litchy
- , Benjamin Boes
- , Elizabeth J Atkinson
- , Sumit Middha
- , P James B Dyck
- , Joseph E Parisi
- , Georges Mer
- , David I Smith
- & Peter J Dyck
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Research | | Open
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The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat
- Ursula M Smith
- , Mark Consugar
- , Louise J Tee
- , Brandy M McKee
- , Esther N Maina
- , Shelly Whelan
- , Neil V Morgan
- , Erin Goranson
- , Paul Gissen
- , Stacie Lilliquist
- , Irene A Aligianis
- , Christopher J Ward
- , Shanaz Pasha
- , Rachaneekorn Punyashthiti
- , Saghira Malik Sharif
- , Philip A Batman
- , Christopher P Bennett
- , C Geoffrey Woods
- , Carole McKeown
- , Martine Bucourt
- , Caroline A Miller
- , Phillip Cox
- , Lihadh AlGazali
- , Richard C Trembath
- , Vicente E Torres
- , Tania Attie-Bitach
- , Deirdre A Kelly
- , Eamonn R Maher
- , Vincent H Gattone II
- , Peter C Harris
- & Colin A Johnson
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Research | | Open
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