Work

Mutations in TPRN Cause a Progressive Form of Autosomal-Recessive Nonsyndromic Hearing Loss

Year: 2010

Type: article

Study design: Observational Study

Source: The American Journal of Human Genetics

DOI: 10.1016/j.ajhg.2010.02.003

Authors: Yun Li, Esther Pohl, Redouane Boulouiz, Margit Schraders, Gudrun Nürnberg, Majida Charif, Ronald J.C. Admiraal, Simon von Ameln, Ingelore Baessmann, Mostafa Kandil, Joris A. Veltman, Peter Nürnberg, Christian Kubisch, Abdelhamid Barakat, Hannie Kremer, Bernd Wollnik

Institutions: University of Cologne, Institut Pasteur du Maroc, Radboud University Nijmegen, Radboud University Medical Center, Donders Institute for Brain, Cognition and Behaviour, Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases, Chouaib Doukkali University

Language: English

Topic: Hearing, Cochlea, Tinnitus, Genetics

Subfield: Sensory Systems

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: European Commission, Bundesministerium für Bildung und Forschung, Fonds NutsOhra, Royal National Institute for Deaf People

Awards: G3741018874, G4854149836, Verbundprojekt: Internationales Netzwerk für kraniofaziale Malformationen (CRANIRARE): Teilprojekt Köln

OpenAlex ID: W1968470805

FWCI: 3.443

Cites: 21

Cited by: 57

Related to: 10