Relevance of SOX17 Variants for Hypomyelinating Leukodystrophies and Congenital Anomalies of the Kidney and Urinary Tract (CAKUT).

Autor:	Combes, Patricia1,2, Planche, Vincent1, Eymard-Pierre, Eléonore1,2, Sarret, Catherine1,3,4, Rodriguez, Diana5, Boespflug-Tanguy, Odile1,6,7, Vaurs-Barriere, Catherine1,4
Zdroj:	Annals of Human Genetics. May2012, Vol. 76 Issue 3, p261-267. 7p.
Databáze:	Academic Search Ultimate
Externí odkaz:	Zobrazit plný text záznamu