(Q35087752)

6 August 2017

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title

Hypertrophic cardiomyopathy: from gene defect to clinical disease (English)

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hypertrophic cardiomyopathy

6 August 2017

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inferred from title

author

Christopher Semsarian

series ordinal

3

object named as

Christopher Semsarian

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6 August 2017

Man-Wei Chung

1

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PubMed ID

12643345

6 August 2017

Tatiana Tsoutsman

series ordinal

2

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6 August 2017

1 February 2003

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6 August 2017

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6 August 2017

13

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6 August 2017

1

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6 August 2017

9-20

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https://scigraph.springernature.com/pub.10.1038/sj.cr.7290146

6 August 2017

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Hypertrophic cardiomyopathy: histopathological features of sudden death in cardiac troponin T disease

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7 January 2021

Patients with familial hypertrophic cardiomyopathy caused by a Phe110Ile missense mutation in the cardiac troponin T gene have variable cardiac morphologies and a favorable prognosis

1 reference

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7 January 2021

Clinical features of hypertrophic cardiomyopathy caused by a Lys183 deletion mutation in the cardiac troponin I gene

1 reference

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7 January 2021

Hypertrophic nonobstructive cardiomyopathy with giant negative T waves (apical hypertrophy): Ventriculographic and echocardiographic features in 30 patients

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CR.7290146

7 January 2021

Direct, convergent hypersensitivity of calcium-activated force generation produced by hypertrophic cardiomyopathy mutant alpha-tropomyosins in adult cardiac myocytes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CR.7290146

7 January 2021

Transgenic modeling of a cardiac troponin I mutation linked to familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CR.7290146

7 January 2021

Comparison of two murine models of familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CR.7290146

7 January 2021

Identifiers

DOI

10.1038/SJ.CR.7290146

1 reference

6 August 2017

1 reference

PubMed ID

12643345