Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, α-dystrobrevin and FK Binding Protein-12

Molecular Genetics and Metabolism

Volumn 82, Issue 2, 2004, Pages 162-166

  Kenton, Alexander B ^a   Sanchez, Ximena ^a   Coveler, Karen J ^a   Makar, Kimberly A ^a   Jimenez, Shinawe ^a   Ichida, Fukiko ^b   Murphy, Ross T ^c   Elliott, Perry M ^c   McKenna, William ^c   Bowles, Neil E ^a   Towbin, Jeffrey A ^a,d   Bowles, Karla R ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF TOYAMA   (Japan)

^c ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

^d FC43009   (United States)

Author keywords

dystrobrevin; FK Binding Protein 12; G4.5; Left ventricular noncompaction; Mutation analysis

Indexed keywords

ALPHA DYSTROBREVIN; BINDING PROTEIN; BINDING PROTEIN 12; DYSTROBREVIN; MESSENGER RNA; UNCLASSIFIED DRUG;

ARTICLE; CARDIOMYOPATHY; CONTROLLED STUDY; DELETION MUTANT; EXON; GENE FREQUENCY; GENE ISOLATION; GENE MUTATION; HEART DISEASE; HUMAN; HUMAN CELL; INTRON; ISOLATED LEFT VENTRICULAR NONCOMPACTION; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; SITE DIRECTED MUTAGENESIS;

BASE SEQUENCE; DYSTROPHIN-ASSOCIATED PROTEINS; HUMANS; HYPERTROPHY, LEFT VENTRICULAR; MUTATION; PROTEINS; RNA SPLICE SITES; RNA, MESSENGER; TACROLIMUS BINDING PROTEIN 1A; TRANSCRIPTION FACTORS;

EID: 2542486394     PISSN: 10967192     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ymgme.2004.02.009     Document Type: Article

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