TY  - GEN
AU  - Zhang,Q-J
AU  - Han,B
AU  - Lan,L
AU  - Zong,L
AU  - Shi,W
AU  - Wang,H-Y
AU  - Xie,L-Y
AU  - Wang,H
AU  - Zhao,C
AU  - Zhang,C
AU  - Yin,Z-F
AU  - Wang,D-Y
AU  - Petit,C
AU  - Guan,J
AU  - Wang,Q-J
TI  - High frequency of OTOF mutations in Chinese infants with congenital auditory neuropathy spectrum disorder
SN  - 1399-0004
PY  - 2017///0630
KW  - Alleles
KW  - Audiometry
KW  - Child
KW  - Child, Preschool
KW  - China
KW  - Female
KW  - Genetic Predisposition to Disease
KW  - Hearing Disorders
KW  - diagnosis
KW  - Hearing Loss, Central
KW  - Humans
KW  - Infant
KW  - Male
KW  - Membrane Proteins
KW  - genetics
KW  - Mutation
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/cge.12744
ER  -