Work

Mutations in PAX3 that cause Waardenburg syndrome type I: Ten new mutations and review of the literature

Year: 1995

Type: review

Source: American Journal of Medical Genetics

DOI: 10.1002/ajmg.1320580205

Authors: Clinton T. Baldwin, Christopher F. Hoth, Roberto A. Macina, Aubrey Milunsky

Institutions: Boston University, The Wistar Institute

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: MOLECULAR GENETICS OF HEARING LOSS--WAARDENBURG SYNDROME, G4019523483

OpenAlex ID: W2117916454

FWCI: 0.677

Cites: 48

Cited by: 129

Related to: 10