Work

Involvement ofDFNB59 mutations in autosomal recessive nonsyndromic hearing impairment

Year: 2007

Type: article

Study design: Observational Study

Source: Human Mutation

DOI: 10.1002/humu.20510

Authors: Rob W.J. Collin, Ersan Kalay, Jaap Oostrik, Refik Çaylan, Bernd Wollnik, Selçuk Arslan, Anneke I. den Hollander, Yelda Birinci, Peter Lichtner, Tim M. Strom, Bayram Toraman, Lies H. Hoefsloot, Cor W.R.J. Cremers, Han G. Brunner, Frans P.M. Cremers, Ahmet Karaguzel, Hannie Kremer

Institutions: Radboud University Medical Center, Karadeniz Technical University, University of Cologne, Istanbul University, Helmholtz Munich, Institut für Humangenetik, TUM Klinikum, Technical University of Munich

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: Oklahoma Agricultural Experiment Station

OpenAlex ID: W2089956906

FWCI: 1.047

Cites: 12

Cited by: 69

Related to: 10