High frequency of OTOF mutations in Chinese infants with congenital auditory neuropathy spectrum disorder.
Zhang, Q-J
High frequency of OTOF mutations in Chinese infants with congenital auditory neuropathy spectrum disorder. [electronic resource] - Clinical genetics 09 2016 - 238-46 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1399-0004
10.1111/cge.12744 doi
Alleles
Audiometry
Child
Child, Preschool
China
Female
Genetic Predisposition to Disease
Hearing Disorders--diagnosis
Hearing Loss, Central--diagnosis
Humans
Infant
Male
Membrane Proteins--genetics
Mutation
High frequency of OTOF mutations in Chinese infants with congenital auditory neuropathy spectrum disorder. [electronic resource] - Clinical genetics 09 2016 - 238-46 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1399-0004
10.1111/cge.12744 doi
Alleles
Audiometry
Child
Child, Preschool
China
Female
Genetic Predisposition to Disease
Hearing Disorders--diagnosis
Hearing Loss, Central--diagnosis
Humans
Infant
Male
Membrane Proteins--genetics
Mutation