A malignant phenotype of hypertrophic cardiomyopathy caused by Arg719Gln cardiac beta-myosin heavy-chain mutation in a Chinese family

Clinica Chimica Acta

Volumn 310, Issue 2, 2001, Pages 131-139

  Huang, X ^a   Song, L ^a   Ma, A Q ^b   Gao, J ^a   Zheng, W ^a   Zhou, X ^a   Zhang, Q ^a   Lu, H ^a   Li, Y ^a   Liu, Y ^a   Hui, R ^a  

^a PEKING UNION MEDICAL COLLEGE   (China)

^b THE FIRST AFFILIATED HOSPITAL OF XI AN JIAOTONG UNIVERSITY   (China)

Author keywords

Gene mutation; Hypertrophic cardiomyopathy; Polymerase chain reaction; Single strand conformation polymorphism; Myosin heavy chain

Indexed keywords

ARGININE; GLUTAMINE; MYOSIN HEAVY CHAIN;

ADULT; ARTICLE; CASE REPORT; CHINA; CODON; CORRELATION FUNCTION; ECHOCARDIOGRAPHY; EXON; FEMALE; GENE MUTATION; HEART ATRIUM ENLARGEMENT; HEART ATRIUM FIBRILLATION; HEART LEFT VENTRICLE OUTFLOW TRACT; HEART PALPITATION; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; MISSENSE MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROGNOSIS; SINGLE STRAND CONFORMATION POLYMORPHISM; SYNCOPE; THORAX PAIN; VERTIGO;

ADULT; AGED; AGED, 80 AND OVER; AMINO ACID SEQUENCE; BASE SEQUENCE; CARDIOMYOPATHY, HYPERTROPHIC; CHILD; CHINA; DNA; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION, MISSENSE; MYOSIN HEAVY CHAINS; PEDIGREE; PHENOTYPE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 0035921154     PISSN: 00098981     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0009-8981(01)00538-1     Document Type: Article

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