Work

Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan

Year: 2007

Type: article

Study design: Observational Study

Source: Clinical Genetics

DOI: 10.1111/j.1399-0004.2007.00895.x

Authors: S‐i Kitajiri, R McNamara, T Makishima, T Husnain, AU Zafar, RA Kittles, ZM Ahmed, TB Friedman, S Riazuddin, AJ Griffith

Institutions: National Institutes of Health, National Institute on Deafness and Other Communication Disorders, The University of Texas Medical Branch at Galveston, University of the Punjab, Centre of Excellence in Molecular Biology, University of Chicago

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

Funders: National Institutes of Health, Japan Society for the Promotion of Science, National Institute of Neurological Disorders and Stroke

OpenAlex ID: W2091199014

FWCI: 2.192

Cites: 17

Cited by: 70

Related to: 10