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A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance
journal contribution
posted on 2023-05-16, 15:19 authored by Kathryn BurdonKathryn Burdon, Wirth, MG, David MackeyDavid Mackey, Russell-Eggitt, IM, Jamie CraigJamie Craig, Elder, JE, Joanne DickinsonJoanne Dickinson, Sale, MMNo description available
History
Publication title
Journal of Medical GeneticsVolume
41Issue
8Pagination
e106-109ISSN
0022-2593Department/School
Menzies Institute for Medical ResearchPublisher
B M J PUBLISHING GROUPPlace of publication
London EnglandRepository Status
- Restricted
