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PMID: 9354784 Published · ppublish English Letter Research Support, Non-U.S. Gov't

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene.

Nature genetics ·Vol. 17 ·No. 3 ·1997-11-00 ·Pages 268-9

Liu XZ, Walsh J, Tamagawa Y, Kitamura K, Nishizawa M, Steel KP, Brown SD

Abstract

暂无摘要

MeSH Terms

Deafness/genetics Genes, Dominant Heterozygote Humans Mutation Myosins/genetics,metabolism Polymorphism, Single-Stranded Conformational Sequence Deletion

Chemicals

Myosins

Authors & Affiliations

7 authors, click to expand affiliations / ORCID

Liu X Z

Walsh J

Tamagawa Y

Kitamura K

Nishizawa M

Steel K P

Brown S D

Article Info

Journal

Nature genetics

Abbr.

Nat Genet

ISSN

1061-4036

DOI

10.1038/ng1197-268

Published

1997-11-00

Pages

268-9

Language

English

Region

United States

NLM ID

9216904

Subset

External Links

PubMed source DOI: 10.1038/ng1197-268 View journal details

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Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene.

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