A do novo mutation in α-tropomyosin that causes hypertrophic cardiomyopathy
- Auteur
- WATKINS, H1 ; ANAN, R1 ; COVIELLO, D. A; SPIRITO, P; SEIDMAN, J. G; SEIDMAN, C. E1
[1] Brigham women's hosp., cardiology div., Boston MA, United States - Source
Circulation (New York, N.Y.). 1995, Vol 91, Num 9, pp 2302-2305 ; ref : 19 ref
- CODEN
- CIRCAZ
- ISSN
- 0009-7322
- Domaine scientifique
- Cardiology, blood circulation, phlebology
- Editeur
- Lippincott Williams & Wilkins, Hagerstown, MD
- Pays de publication
- United States
- Type de document
- Article
- Langue
- English
- Mot clé (fr)
- Cardiomyopathie hypertrophique Exploration Gène Homme Mutation Tropomyosine Appareil circulatoire pathologie Cardiopathie Myocarde pathologie
- Mot clé (en)
- Hypertrophic cardiomyopathy Exploration Gene Human Mutation Tropomyosin Cardiovascular disease Heart disease Myocardial disease
- Mot clé (es)
- Cardiomiopatía hipertrófica Exploración Gen Hombre Mutación Tropomiosina Aparato circulatorio patología Cardiopatía Miocardio patología
- Classification
- Pascal
- 002 Sciences biologiques et medicales / 002B Sciences medicales / 002B12 Cardiologie. Appareil circulatoire / 002B12A Coeur / 002B12A05 Myocardites. Cardiomyopathies
- Discipline
- Cardiology. Circulatory system
- Provenance
- Inist-CNRS
- Base de données
- PASCAL
- Identifiant INIST
- 3522498
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
10.1161/01.CIR.91.9.2302 
https://dx.doi.org/10.1161/01.CIR.91.9.2302
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