Defective myosin VIIA gene responsible for Usher syndrome type IB

Nature

Volumn 374, Issue 6517, 1995, Pages 60-61

  Well, Dominique ^a   Blanchard, Stéphane ^a   Kaplan, Josseline ^b   Guilford, Parry ^a   Gibson, Fernando ^c   Walsh, James ^c   Mburu, Philomena ^c   Varela, Anabel ^c   Levilliers, Jacqueline ^a   Weston, Michael D ^d   Kelley, Phillip M ^d   Kimberling, William J ^d   Wagenaar, Mariette ^e   Levi Acobas, Fabienne ^a   Larget Piet, Dominique ^b   Munnich, Arnold ^b   Steel, Karen P ^f   Brown, Steve D M ^c   Petit, Christine ^a  

^a INSTITUT PASTEUR   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c IMPERIAL COLLEGE LONDON   (United Kingdom)

^d BOYS TOWN NATIONAL RESEARCH HOSPITAL   (United States)

^e RADBOUD UNIVERSITY NIJMEGEN   (Netherlands)

^f MRC INSTITUTE OF HEARING RESEARCH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOSKELETON PROTEIN; MYOSIN;

ALLELE; AMINO TERMINAL SEQUENCE; ANIMAL TISSUE; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; AXONEME; CHROMOSOME 11Q; CONTROLLED STUDY; CORTI ORGAN; CYTOSKELETON; GENE DELETION; GENE MAPPING; GENE MUTATION; HEARING IMPAIRMENT; HUMAN; HUMAN TISSUE; MICROTUBULE; MOUSE; NONHUMAN; NOSE CAVITY; PERCEPTION DEAFNESS; PHOTORECEPTOR; PRIORITY JOURNAL; PROTEIN DOMAIN; PSEUDOPODIUM; RETINITIS PIGMENTOSA; SPERM; STOP CODON; USHER SYNDROME; VESTIBULAR DISORDER;

ADULT; AMINO ACID SEQUENCE; ANIMAL; BASE SEQUENCE; CHILD; CHROMOSOMES, HUMAN, PAIR 11; DEAFNESS; DNA; DNA MUTATIONAL ANALYSIS; FEMALE; HUMAN; MALE; MICE; MOLECULAR SEQUENCE DATA; MUTATION; MYOSINS; RETINITIS PIGMENTOSA; SEQUENCE HOMOLOGY, AMINO ACID; SUPPORT, NON-U.S. GOV'T; SWINE; SYNDROME;

EID: 0028815440     PISSN: 00280836     EISSN: None     Source Type: Journal    
DOI: 10.1038/374060a0     Document Type: Article

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