Work

High frequency hearing loss correlated with mutations in the GJB2 gene

Year: 2000

Type: article

Study design: Observational Study

Source: Human Genetics

DOI: 10.1007/s004390000273

Authors: Stephen A Wilcox, Kerryn Saunders, Amelia H Osborn, Angela Arnold, Julia Wunderlich, Therese Kelly, Veronica Collins, Leah J Wilcox, RJ McKinlay Gardner, Maria Kamarinos, Barbara Cone-Wesson, Robert Williamson, Hans-Henrik M. Dahl

Institutions: Royal Children's Hospital, Monash Medical Centre, Monash University, Monash Health, The University of Melbourne

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: Garnett Passe and Rodney Williams Memorial Foundation, National Health and Medical Research Council, National Medical Research Council

OpenAlex ID: W1999640231

FWCI: 5.885

Cites:

Cited by: 201

Related to: 10