Work

Dominant modifier DFNM1 suppresses recessive deafness DFNB26

Year: 2000

Type: article

Study design: Observational Study

Source: Nature Genetics

DOI: 10.1038/82558

Authors: Saima Riazuddin, Caley M. Castelein, Zubair M. Ahmed, Anil K. Lalwani, Mary A. Mastroianni, Sadaf Naz, Tenesha N. Smith, Nikki A. Liburd, Thomas B. Friedman, Andrew J. Griffith, Sheikh Riazuddin, Edward R. Wilcox

Institutions: National Institutes of Health, National Institute on Deafness and Other Communication Disorders, University of California, San Francisco, University of the Punjab, Centre of Excellence in Molecular Biology

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: National Institute on Deafness and Other Communication Disorders

Awards: G3689424842, Mapping And Cloning Hereditary Hearing Impairment Genes

OpenAlex ID: W1596627530

FWCI: 6.362

Cites: 30

Cited by: 140

Related to: 10