Work

Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing

Year: 2013

Type: article

Study design: Observational Study

Source: European Journal of Human Genetics

DOI: 10.1038/ejhg.2013.232

Authors: Zippora Brownstein, Amal Abu-Rayyan, Daphne Karfunkel-Doron, Serena Sirigu, Bella Davidov, Mordechai Shohat, Moshe Frydman, Anne Houdusse, Moien Kanaan, Karen B Avraham

Institutions: Tel Aviv University, Bethlehem University, Centre National de la Recherche Scientifique, Biologie cellulaire et Cancer, Institut Curie, Rabin Medical Center, Sheba Medical 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: bronze

Funders: Science Foundation Ireland, Agence Nationale de la Recherche, National Institutes of Health, Israeli Centers for Research Excellence, National Institute on Deafness and Other Communication Disorders

Awards: G4791905715, G6722458753, Genomic Approaches to Discovery and Characterization of Genes for Inherited Hearing Loss

OpenAlex ID: W2054895513

FWCI: 2.305

Cites: 47

Cited by: 49

Related to: 10