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

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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Bibliographic Details
Main Authors: Masoumeh Mohebi, Saeed Chenari, Abolfazl Akbari, Fariba Ghassemi, Mehran Zarei-Ghanavati, Ghasem Fakhraie, Nahid Babaie, Mansour Heidari
Format: Article
Language:English
Published: Mashhad University of Medical Sciences 2017-03-01
Series:Iranian Journal of Basic Medical Sciences
Subjects:
Cataract
Congenital
Connexine 50 gene
GJA8
Mutation
Online Access:http://ijbms.mums.ac.ir/article_8358_b07ad559443877d8ee1da6ef6617064c.pdf

Internet

http://ijbms.mums.ac.ir/article_8358_b07ad559443877d8ee1da6ef6617064c.pdf

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