Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy

Circulation Research

Volumn 80, Issue 3, 1997, Pages 427-434

  Carrier, Lucie ^a   Bonne, Gisèle ^a   Bährend, Ellen ^a   Yu, Bing ^f   Richard, Pascale ^a   Niel, Florence ^a   Hainque, Bernard ^a   Cruaud, Corinne ^d   Gary, Françoise ^d   Labeit, Siegfried ^e   Bouhour, Jean Brieuc ^g   Dubourg, Olivier ^b   Desnos, Michel ^c   Hagège, Albert A ^c   Trent, Ronald J ^f   Komajda, Michel ^a   Fiszman, Marc ^a   Schwartz, Ketty ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b HÔPITAL AMBROISE PARÉ   (France)

^c Hopital Boucicaut   (France)

^d GÉNÉTHON   (France)

^e EMBL   (Germany)

^f ROYAL PRINCE ALFRED HOSPITAL   (Australia)

^g NONE

Author keywords

cardiomyopathy; contractile protein; genetics; hypertrophy; myosin binding protein

Indexed keywords

MUSCLE PROTEIN; MYOSIN; MYOSIN BINDING PROTEIN C; UNCLASSIFIED DRUG;

ARTICLE; BASE PAIRING; EXON; GENE MUTATION; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0031055854     PISSN: 00097330     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.res.0000435859.24609.b3     Document Type: Article

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