(Q47801133)

5 February 2018

title

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy. (English)

1 reference

5 February 2018

author name string

Ross T Murphy

1

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5 February 2018

Jens Mogensen

2

1 reference

5 February 2018

Anthony Shaw

3

1 reference

5 February 2018

Toru Kubo

4

1 reference

5 February 2018

Sian Hughes

5

1 reference

5 February 2018

William J McKenna

6

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5 February 2018

language of work or name

English

0 references

publication date

1 January 2004

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5 February 2018

published in

The Lancet

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5 February 2018

volume

363

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5 February 2018

page(s)

371-372

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5 February 2018

issue

9406

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5 February 2018

Molecular genetics of left ventricular dysfunction

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915468-8

7 January 2021

Familial dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915468-8

7 January 2021

Comparison of fluorescent SSCP and denaturing HPLC analysis with direct sequencing for mutation screening in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915468-8

7 January 2021

Interactions at the NH2-terminal interface of cardiac troponin I modulate myofilament activation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915468-8

7 January 2021

Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915468-8

7 January 2021

10.1016/S0140-6736(04)15468-8

Identifiers

DOI

1 reference

5 February 2018

PubMed ID

15070570

1 reference

5 February 2018