Work

DFNB3, Spectrum of MYO15A Recessive Mutant Alleles and an Emerging Genotype-Phenotype Correlation

Year: 2002

Type: book-chapter

Study design: Observational Study

Source: KARGER eBooks

DOI: 10.1159/000066824

Authors: T.B. Friedman, J.T. Hinnant, M. Ghosh, E.T. Boger, S. Riazuddin, J.R. Lupski, L. Potocki, E.R. Wilcox

Institutions: National Institutes of Health, National Institute on Deafness and Other Communication Disorders, Michigan State University, All India Institute of Medical Sciences, Centre of Excellence in Molecular Biology, Baylor College of Medicine, Texas Children's Hospital

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, National Institute on Deafness and Other Communication Disorders

Awards: Mapping And Cloning Hereditary Hearing Impairment Genes, Positional Cloning of DFNB3 Reveals a Novel Unconventional Myosin, MYO15, G7141115367, G7416650997

OpenAlex ID: W1595373911

FWCI: 0.959

Cites:

Cited by: 19

Related to: 10