Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice

Human Molecular Genetics

Volumn 6, Issue 8, 1997, Pages 1225-1231

  Avraham, Karen B ^a   Hasson, Tama ^b   Sobe, Tama ^a   Balsara, Binaifer ^c   Testa, Joseph R ^c   Skvorak, Anne B ^d   Morton, Cynthia C ^d   Copeland, Neal G ^e   Jenkins, Nancy A ^e  

^a TEL AVIV UNIVERSITY   (Israel)

^b YALE UNIVERSITY   (United States)

^c FOX CHASE CANCER CENTER   (United States)

^d BRIGHAM AND WOMEN S HOSPITAL   (United States)

^e NATIONAL CANCER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; MYOSIN;

ANIMAL TISSUE; ARTICLE; CHROMOSOME 6Q; FEMALE; FETUS; GENE DELETION; GENE ISOLATION; GENE MAPPING; HEARING IMPAIRMENT; HUMAN; HUMAN CELL; HUMAN TISSUE; MOLECULAR CLONING; MOUSE; MOUSE MUTANT; NONHUMAN; NORMAL HUMAN; PRIORITY JOURNAL; SEQUENCE HOMOLOGY;

AMINO ACID SEQUENCE; ANIMALS; CHROMOSOMES, HUMAN, PAIR 6; DEAFNESS; FEMALE; HUMANS; MICE; MOLECULAR SEQUENCE DATA; MYOSIN HEAVY CHAINS;

ANIMALIA;

EID: 0030751937     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/6.8.1225     Document Type: Article

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