Whole exome sequencing reveals pathogenic variants in MYO3A, MYO15A and COL9A3 and differential frequencies in ancestral alleles in hearing impairment genes among individuals from Cameroon.
Human molecular genetics 2020 Oct .
Wonkam Ambroise, Manyisa Noluthando, Bope Christian D, Dandara Collet, Chimusa Emile
Mutation analysis of COL9A3, a gene highly expressed in the cochlea, in hearing loss patients.
Auris, nasus, larynx 2005 Jun 32 (2): 113-7.
Asamura Kenji, Abe Satoko, Fukuoka Hisakuni, Nakamura Yusuke, Usami Shin-ic