Homozygosity mapping identifies a novel GIPC3 mutation causing congenital nonsyndromic hearing loss in a Saudi family
Ramzan, Khushnooda, Al-Owain, Mohammed, Allam, Rabab, Berhan, Amal, Abuharb, Gheid, Taibah, Khalid, Imtiaz, FaiqaVolume:
521
Language:
english
Journal:
Gene
DOI:
10.1016/j.gene.2013.03.042
Date:
May, 2013
File:
PDF, 842 KB
english, 2013