A Missense Mutation in RAB28 in a Family with Cone-Rod Dystrophy and Postaxial Polydactyly Prevents Localization of RAB28 to the Primary Cilium

PURPOSE: Cone-rod dystrophy (CRD) is a rare hereditary eye disorder that causes progressive degeneration of cone and rod photoreceptors. More than 30 genes, including RAB28, have been associated with CRD; however, only a few RAB28 variants have been reported to be associated with CRD. In this study,...

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محفوظ في:
التفاصيل البيبلوغرافية
الحاوية / القاعدة:Invest Ophthalmol Vis Sci
المؤلفون الرئيسيون: Jespersgaard, Cathrine, Hey, Amalie Brunbjerg, Ilginis, Tomas, Hjortshøj, Tina Duelund, Fang, Mingyan, Bertelsen, Mette, Bech, Niels, Jensen, Hanne, Larsen, Lasse Jonsgaard, Tümer, Zeynep, Rosenberg, Thomas, Brøndum-Nielsen, Karen, Møller, Lisbeth Birk, Grønskov, Karen
التنسيق: Artigo
اللغة:Inglês
منشور في: The Association for Research in Vision and Ophthalmology 2020
الموضوعات:
Genetics
الوصول للمادة أونلاين:https://ncbi.nlm.nih.gov/pmc/articles/PMC7326575/
https://ncbi.nlm.nih.gov/pubmed/32084271
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.61.2.29
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