Work

A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian family

Year: 1992

Type: article

Source: Human Molecular Genetics

DOI: 10.1093/hmg/1.4.243

Authors: Robert Morell, Thomas B. Friedman, Sukarti Moeljopawiro, Hartono, Soewito, James H. Asher

Institutions: Michigan State University, Universitas Gadjah Mada

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: DEAFNESS AND WAARDENBURG SYNDROME

OpenAlex ID: W2098533677

FWCI: 8.78

Cites:

Cited by: 88

Related to: 10