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 |
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Zdroj: | Cell Journal (Yakhteh). Jul-sep2018, Vol. 20 Issue 2, p290-292. 3p. |
Databáze: | Academic Search Ultimate |
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