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

Nature Genetics

Volumn 17, Issue 3, 1997, Pages 268-269

  Liu, Xue Zhong ^a   Walsh, James ^a   Tamagawa, Yuya ^c   Kitamura, Ken ^c   Nishizawa, Masatoyo ^d   Steel, Karen P ^e   Brown, Steve D M ^a,b  

^a MRC Mouse Genome Centre   (United Kingdom)

^b MRC MAMMALIAN GENETICS UNIT   (United Kingdom)

^c Department of Otolaryngology ^*  (Japan)

^d JICHI MEDICAL UNIVERSITY   (Japan)

^e MRC INSTITUTE OF HEARING RESEARCH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN;

DOMINANT GENE; GENE DELETION; GENETICS; HEARING IMPAIRMENT; HETEROZYGOTE; HUMAN; LETTER; METABOLISM; MUTATION; SINGLE STRAND CONFORMATION POLYMORPHISM;

DEAFNESS; GENES, DOMINANT; HETEROZYGOTE; HUMANS; MUTATION; MYOSINS; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SEQUENCE DELETION;

EID: 0031278277     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng1197-268     Document Type: Letter

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