Genetic analysis of a consanguineous Pakistani family with Leber congenital amaurosis identifies a novel mutation in GUCY2D gene.

Autor: KHAN, MUZAMMIL1, RUPP, VERENA2, KHAN, MUHAMMAD1,3, ANSAR, MUHAMMAD4, WINDPASSINGER, CHRISTIAN2 christian.windpassinger@medunigraz.at
Zdroj: Journal of Genetics. Jul2014, Vol. 93 Issue 2, p527-530. 4p.
Databáze: Academic Search Ultimate