Congenital deafness: high prevalence of a V37I mutation in the GJB2 gene among deaf school children in Alor Setar.

Autor: Ruszymah BH; Department of Physiology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Jalan Raja Muda Abdul Aziz, Kuala Lumpur., Wahida IF, Zakinah Y, Zahari Z, Norazlinda MD, Saim L, Aminuddin BS

Publikováno v: The Medical journal of Malaysia [Med J Malaysia] 2005 Aug; Vol. 60 (3), pp. 269-74.