Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy (Q47801133)

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English	Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/15070570

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

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/15070570

author name string

Ross T Murphy

1

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/15070570

Jens Mogensen

2

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/15070570

Anthony Shaw

3

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/15070570

Toru Kubo

4

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/15070570

Sian Hughes

5

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/15070570

William J McKenna

6

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/15070570

language of work or name

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publication date

1 January 2004

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/15070570

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/15070570

363

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/15070570

9406

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/15070570

371-372

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/15070570

Molecular genetics of left ventricular dysfunction

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial dilated cardiomyopathy

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0140-6736(04)15468-8

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/15070570

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/15070570

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