Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9

American Journal of Human Genetics

Volumn 67, Issue 5, 2000, Pages 1121-1128

  Lalwani, Anil K ^a   Goldstein, Jayne A ^a   Kelley, Michael J ^b   Luxford, William ^c   Castelein, Caley M ^a   Mhatre, Anand N ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b DUKE UNIVERSITY MEDICAL CENTER   (United States)

^c HOUSE EAR INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN;

AMINO ACID SUBSTITUTION; ANIMAL TISSUE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; COCHLEA; GENE MAPPING; GENE SEQUENCE; HEARING IMPAIRMENT; HUMAN; IMMUNOHISTOCHEMISTRY; MISSENSE MUTATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS; TISSUE DISTRIBUTION;

ANIMALIA;

EID: 0033764817     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9297(07)62942-5     Document Type: Article

References (31)

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