Work

Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorder

Year: 2005

Type: article

Source: Human Genetics

DOI: 10.1007/s00439-005-0001-4

Authors: Tomoko Makishima, Clara I. Rodriguez, Nahid G. Robertson, Cynthia C. Morton, Colin L. Stewart, Andrew J. Griffith

Institutions: National Institutes of Health, National Institute on Deafness and Other Communication Disorders, National Cancer Institute, Brigham and Women's Hospital, Harvard University

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

Funders: National Institutes of Health, National Institute on Deafness and Other Communication Disorders

Awards: Cloning Genes Involved in Hearing, Molecular Analysis Of Human Hereditary Deafness, G8000224386

OpenAlex ID: W2074093860

FWCI: 1.264

Cites: 26

Cited by: 35

Related to: 10