INSTITUTION'S PROFILE

UF Innovation en Diagnostic Genomique des Maladies Rares, CHU Dijon Bourgogne, Dijon, France.

Publications (1)

Variants of human CLDN9 cause mild to profound hearing loss.

Journal: Human mutation

Publication date: 2022

Journal: Human mutation

Publication Year: 2022

Authors & Co-authors:  Ramzan Memoona M Philippe Christophe C Belyantseva Inna A IA Nakano Yoko Y Fenollar-Ferrer Cristina C Tona Risa R Yousaf Rizwan R Basheer Rasheeda R Imtiaz Ayesha A Faridi Rabia R