Identification of A Novel Missense Mutation in The Norrie Disease Gene: The First Molecular Genetic Analysis and Prenatal Diagnosis of Norrie Disease in An Iranian Family.

Autor: Talebi, Farah1, Mardasi, Farideh Ghanbari2 ghanbari246@gmail.com, Mohammadi, Javad3, Lashgari, Ali4, Farhadi, Freidoon5
Zdroj: Cell Journal (Yakhteh). Jul-sep2018, Vol. 20 Issue 2, p290-292. 3p.
Databáze: Academic Search Ultimate