Genomic structure of the human unconventional myosin VI gene

Gene

Volumn 261, Issue 2, 2000, Pages 269-275

  Ahituv, Nadav ^a   Sobe, Tama ^a   Robertson, Nahid G ^b   Morton, Cynthia C ^b   Taggart, R Thomas ^c   Avraham, Karen B ^a  

^a TEL AVIV UNIVERSITY   (Israel)

^b BRIGHAM AND WOMEN S HOSPITAL   (United States)

^c UNIVERSITY AT BUFFALO   (United States)

Author keywords

Deafness; Non syndromic hearing loss; Snell's waltzer

Indexed keywords

AMINO ACID; MYOSIN; MYOSIN VI; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ARTICLE; CHROMOSOME 6Q; DNA POLYMORPHISM; EXON; GENE MAPPING; GENE STRUCTURE; GENOME; HEARING LOSS; HUMAN; PRIORITY JOURNAL; RETINOPATHY; SCREENING TEST; SINGLE STRAND CONFORMATION POLYMORPHISM; USHER SYNDROME;

ADULT; BASE SEQUENCE; BRAIN; DEAFNESS; DNA; DNA MUTATIONAL ANALYSIS; EXONS; FAMILY HEALTH; FETUS; GENE FREQUENCY; GENES; HUMANS; INTRONS; MUTATION; MYOSIN HEAVY CHAINS; POINT MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 0034739798     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1119(00)00535-7     Document Type: Article

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