Early expression of a malignant phenotype of familial hypertrophic cardiomyopathy associated with a Gly716Arg myosin heavy chain mutation in a Korean family
- Author
- HWANG, T.-H; LEE, W.-H; KIMURA, A; SATOH, M; NAKAMURA, T; KIM, M.-K; CHOI, S.-K; PARK, J.-E
Cardiology Division, Samsung Medical Center, College of Medicine, Sung Kyun Kwan University, Seoul, Korea, Republic of
Department of Internal Medicine, University of Inje, Seoul Paik Hospital, Seoul, Korea, Republic of
Department of Tissue Physiology, Division of Adult Diseases, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan
Samsung Biomedical Research Institute, Seoul, Korea, Republic of - Source
The American journal of cardiology. 1998, Vol 82, Num 12, pp 1509-1513 ; ref : 22 ref
- CODEN
- AJCDAG
- ISSN
- 0002-9149
- Scientific domain
- Cardiology, blood circulation, phlebology
- Publisher
- Elsevier, New York, NY
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Cardiomyopathie hypertrophique Chaîne peptidique lourde Chaîne peptidique β Complication Déterminisme génétique Etude familiale Expression génique Gène Homme Insuffisance cardiaque Mort subite Mutation Myosine Phénotype Précoce Pénétrance génique Corée Appareil circulatoire pathologie Biologie moléculaire Cardiopathie Génétique Maladie héréditaire Myocarde pathologie Asie
- Keyword (en)
- Hypertrophic cardiomyopathy Heavy peptide chain Beta-Peptide chain Complication Genetic determinism Family study Gene expression Gene Human Heart failure Sudden death Mutation Myosin Phenotype Early Gene penetrance Korea Cardiovascular disease Molecular biology Heart disease Genetics Genetic disease Myocardial disease Asia
- Keyword (es)
- Cardiomiopatía hipertrófica Cadena peptídica pesada Cadena peptídica β Complicación Determinismo genético Estudio familiar Expresión genética Gen Hombre Insuficiencia cardíaca Muerte súbita Mutación Miosina Fenotipo Precoz Penetrancia génica Corea Aparato circulatorio patología Biología molecular Cardiopatía Genética Enfermedad hereditaria Miocardio patología Asia
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B12 Cardiology. Vascular system / 002B12A Heart / 002B12A05 Myocarditis. Cardiomyopathies
- Discipline
- Cardiology. Circulatory system Tropical medicine
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 1632686
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1016/S0002-9149(98)00695-X 
https://dx.doi.org/10.1016/S0002-9149(98)00695-X
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