Mutation analysis of connexin 50 gene among Iranian families with autosomal dominant cataracts

OBJECTIVE(S): Childhood cataract is a genetically heterogeneous eye disorder that results in visual impairment. The aim of this study was to identify the genetic mutations of connexin 50 gene among Iranian families suffered from autosomal dominant congenital cataracts (ADCC). MATERIALS AND METHODS:...

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Detalles Bibliográficos
Autores principales: Mohebi, Masoumeh, Chenari, Saeed, Akbari, Abolfazl, Ghassemi, Fariba, Zarei-Ghanavati, Mehran, Fakhraie, Ghasem, Babaie, Nahid, Heidari, Mansour
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5378966/
https://www.ncbi.nlm.nih.gov/pubmed/28392901
http://dx.doi.org/10.22038/IJBMS.2017.8358

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5378966/
https://www.ncbi.nlm.nih.gov/pubmed/28392901
http://dx.doi.org/10.22038/IJBMS.2017.8358

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