The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

Nature Genetics

Volumn 16, Issue 2, 1997, Pages 191-193

  Weil, D ^a   Kussel, P ^a   Blanchard, S ^a   Levy, G ^a   Levi Acobas, F ^a   Drira, M ^a   Ayadi, H ^a   Petit, C ^a  

^a CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN;

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOME 11Q; CLINICAL ARTICLE; FEMALE; GENE LOCATION; GENE MUTATION; HEARING IMPAIRMENT; HUMAN; MALE; PRIORITY JOURNAL; USHER SYNDROME;

ALLELES; AMINO ACID SEQUENCE; ANIMALS; DEAFNESS; DYNEIN ATPASE; GENES, RECESSIVE; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; MYOSINS; SEQUENCE HOMOLOGY, AMINO ACID; SYNDROME;

MURINAE;

EID: 0030951102     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0697-191     Document Type: Article

References (28)