Código QR (código de barras bidimensional)

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:...

ver descrição completa

Na minha lista:
Principais autores: Masoumeh Mohebi, Saeed Chenari, Abolfazl Akbari, Fariba Ghassemi, Mehran Zarei-Ghanavati, Ghasem Fakhraie, Nahid Babaie, Mansour Heidari
Formato: Artigo
Idioma:Inglês
Publicado em: Mashhad University of Medical Sciences 2017-03-01
coleção:Iranian Journal of Basic Medical Sciences
Assuntos:
Cataract
Congenital
Connexine 50 gene
GJA8
Mutation
Acesso em linha:http://ijbms.mums.ac.ir/article_8358_b07ad559443877d8ee1da6ef6617064c.pdf
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registros relacionados