Work

A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family

Year: 2008

Type: article

Study design: Observational Study

Source: American Journal of Medical Genetics Part A

DOI: 10.1002/ajmg.a.32174

Authors: Kirsten M. Sanggaard, Klaus W. Kjaer, Hans Eiberg, Gudrun Nürnberg, Peter Nürnberg, Katrin Hoffman, Hanne Jensen, Charlotte Sørum, Nanna D. Rendtorff, Lisbeth Tranebjærg

Institutions: University of Copenhagen, Bispebjerg Hospital, University of Cologne, Humboldt-Universität zu Berlin, Charité – Universitätsmedizin Berlin, Kennedy Center

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

OpenAlex ID: W2008317354

FWCI: 1.432

Cites: 28

Cited by: 45

Related to: 10