The genomic organization of human dystrobrevin

Neurogenetics

Volumn 1, Issue 1, 1997, Pages 37-42

  Sadoulet Puccio, Hélène M ^a   Feener, Chris A ^b   Schaid, Daniel J ^c   Thibodeau, Stephen N ^c   Michels, Virginia V ^c   Kunkel, Louis M ^a,b  

^a HARVARD MEDICAL SCHOOL   (United States)

^b BOSTON CHILDREN S HOSPITAL   (United States)

^c MAYO CLINIC   (United States)

Author keywords

Dystrobrevin; Dystrophin; Dystrophin associated protein; Dystrophin related protein; Neuromuscular junction; SSCP

Indexed keywords

DTNA PROTEIN, HUMAN; DYSTROBREVIN; DYSTROPHIN; DYSTROPHIN ASSOCIATED PROTEIN; NEUROPEPTIDE;

ARTICLE; BIOLOGICAL MODEL; CHROMOSOME 18; EXON; GENE LIBRARY; GENETICS; HEART RIGHT VENTRICLE DYSPLASIA; HUMAN; INTRON; MOLECULAR GENETICS; NORTHERN BLOTTING; NUCLEOTIDE SEQUENCE; SINGLE STRAND CONFORMATION POLYMORPHISM; TISSUE DISTRIBUTION;

ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA; BLOTTING, NORTHERN; CHROMOSOMES, HUMAN, PAIR 18; DNA MUTATIONAL ANALYSIS; DYSTROPHIN; DYSTROPHIN-ASSOCIATED PROTEINS; EXONS; GENE LIBRARY; HUMANS; INTRONS; MODELS, GENETIC; MOLECULAR SEQUENCE DATA; NEUROPEPTIDES; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; TISSUE DISTRIBUTION;

EID: 0031128833     PISSN: 13646745     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100480050006     Document Type: Article

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