Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A).

Autor: Çelmeli, Gamze1 gcelmeli@hotmail.com, Türkkahraman, Doğa2, Çürek, Yusuf1, Houghton, Jayne3, Akçurin, Sema1, Bircan, İffet1
Zdroj: Journal of Clinical Research in Pediatric Endocrinology. Mar2017, Vol. 9 Issue 1, p80-84. 5p.
Databáze: Academic Search Ultimate