Work

Mutation in Transcription Factor POU4F3 Associated with Inherited Progressive Hearing Loss in Humans

Year: 1998

Type: article

Study design: Observational Study

Source: Science

DOI: 10.1126/science.279.5358.1950

Authors: Oz Vahava, Robert Morell, Eric D. Lynch, Sigal Weiss, Marjory E. Kagan, Nadav Ahituv, Jan E. Morrow, Ming K. Lee, Anne B. Skvorak, Cynthia C. Morton, Anat Blumenfeld, Moshe Frydman, Thomas B. Friedman, Mary-Claire King, Karen B. Avraham

Institutions: Brigham and Women's Hospital, National Institutes of Health, Harvard University, Tel Aviv University, University of Washington, Hadassah Medical Center, National Institute on Deafness and Other Communication Disorders

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

Awards: Identification of Genes Causing Syndromic And Nonsyndromic Hearing Impairment, DFNA1 IN INHERITED HEARING LOSS

OpenAlex ID: W2107658807

FWCI: 16.57

Cites: 34

Cited by: 340

Related to: 10