Work

Autosomal Recessive Nonsyndromic Neurosensory Deafness at DFNB1 Not Associated with the Compound-Heterozygous GJB2 (Connexin 26) Genotype M34T/167delT

Year: 2000

Type: article

Study design: Observational Study

Source: The American Journal of Human Genetics

DOI: 10.1086/303045

Authors: Andrew J. Griffith, Aqeel A. Chowdhry, Kiyoto Kurima, Linda J. Hood, Bronya Keats, Charles I. Berlin, Robert J. Morell, Thomas B. Friedman

Institutions: National Institutes of Health, National Institute on Deafness and Other Communication Disorders, Louisiana State University Health Sciences Center New Orleans

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: National Institutes of Health, National Institute on Deafness and Other Communication Disorders

Awards: G1805836306, Research Training in the Language Sciences, Analyses of Type XI Collagen in Craniofacial Development and the Auditory System, G2649043215, G2830933712, G3074743354, Mapping And Cloning Hereditary Hearing Impairment Genes, G6963841607, G8493216334

OpenAlex ID: W1993967715

FWCI: 4.083

Cites: 20

Cited by: 68

Related to: 10