Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

Nature Genetics

Volumn 16, Issue 2, 1997, Pages 188-190

  Liu, X Z ^a   Walsh, J ^a   Mburu, P ^a   Kendrick Jones, J ^a   Cope, M J T V ^a   Steel, K P ^a   Brown, S D M ^a  

^a MRC MAMMALIAN GENETICS UNIT   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN;

ADULT; ARTICLE; CHROMOSOME 11Q; CLINICAL ARTICLE; FAMILY STUDY; FEMALE; GENE LOCATION; GENE MUTATION; HUMAN; MALE; PERCEPTION DEAFNESS; PRIORITY JOURNAL; USHER SYNDROME;

ADULT; ANIMALS; CHROMOSOMES, HUMAN, PAIR 11; DEAFNESS; DYNEIN ATPASE; EXONS; GENES, RECESSIVE; HETEROZYGOTE; HUMANS; MICE; MIDDLE AGED; MUTATION; MYOSINS; PEDIGREE; RNA SPLICING;

EID: 0030960855     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0697-188     Document Type: Article

References (19)