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Sudden death due to troponin T mutations
scientific article
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instance of
scholarly article
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title
Sudden death due to troponin T mutations
(English)
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author
Hugh Christian Watkins
object named as
H Watkins
series ordinal
7
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author name string
J C Moolman
series ordinal
1
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V A Corfield
series ordinal
2
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B Posen
series ordinal
3
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K Ngumbela
series ordinal
4
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C Seidman
series ordinal
5
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P A Brink
series ordinal
6
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language of work or name
English
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publication date
1 March 1997
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published in
Journal of the American College of Cardiology
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volume
29
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page(s)
549-55
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issue
3
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cites work
Causes of sudden death in competitive athletes
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Sudden death from cardiac causes in children and young adults
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Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (1).
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Prognosis in hypertrophic cardiomyopathy: role of age and clinical, electrocardiographic and hemodynamic features
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Sudden death in hypertrophic cardiomyopathy: a profile of 78 patients
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Relation of left ventricular function and prognosis in hypertrophic cardiomyopathy: an angiographic study.
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Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy
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Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy
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Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy
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Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac beta myosin heavy chain gene mutations
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Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy
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Molecular genetics. Therapy or terror?
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Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere
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Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy
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Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy
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Familial hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy
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Identification of a new missense mutation at Arg403, a CpG mutation hotspot, in exon 13 of the beta-myosin heavy chain gene in hypertrophic cardiomyopathy
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Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene
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Sudden cardiac death in hypertrophic cardiomyopathy. Variability in phenotypic expression of beta-myosin heavy chain mutations
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reference URL
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Identifiers
DOI
10.1016/S0735-1097(96)00530-X
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4867449
OpenCitations bibliographic resource ID
4867449
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4867449
PubMed ID
9060892
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4867449
ResearchGate publication ID
14150800
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