Work

Human NDUFB9 Gene: Genomic Organization and a Possible Candidate Gene Associated with Deafness Disorder Mapped to Chromosome 8q13

Year: 1999

Type: article

Source: Human Heredity

DOI: 10.1159/000022848

Authors: Xin Lin, Dan E. Wells, William J. Kimberling, Shrawan Kumar

Institutions: University of Houston, Boys Town National Research Hospital

Language: English

Topic: Hearing, Cochlea, Tinnitus, Genetics

Subfield: Sensory Systems

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: National Institute on Deafness and Other Communication Disorders

Award: GENTICS OF USHER SYNDROME

OpenAlex ID: W2013597883

FWCI: 0.641

Cites: 32

Cited by: 18

Related to: 10