(Q28248327)

5

0 references

Pertti Jääskeläinen

1

object named as

Pertti Jääskeläinen

0 references

Raija Miettinen

2

object named as

Raija Miettinen

0 references

Lauri Toivonen

4

object named as

Lauri Toivonen

0 references

author name string

Päivi Kärkkäinen

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

3

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language of work or name

English

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publication date

2004

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published in

Annals of Medicine

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volume

36

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issue

1

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page(s)

23-32

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cites work

1 reference

https://api.crossref.org/works/10.1080/07853890310017161

The management of hypertrophic cardiomyopathy

21 April 2017

1 reference

https://api.crossref.org/works/10.1080%2F07853890310017161

First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310017161

The molecular genetic basis for hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310017161

Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310017161

Molecular genetic studies of familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310017161

Structural analysis of the titin gene in hypertrophic cardiomyopathy: identification of a novel disease gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310017161

Disease gene mapping in isolated human populations: the example of Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310017161

Molecular genetics of the Finnish disease heritage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310017161

Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310017161

Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310017161

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310017161

Clinical Features of Hypertrophic Cardiomyopathy Caused by Mutation of a “Hot Spot” in the Alpha-Tropomyosin Gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310017161

Hypertrophic cardiomyopathy in Tuscany: clinical course and outcome in an unselected regional population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310017161

Clinical course of hypertrophic cardiomyopathy in a regional United States cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890310017161

10.1080/07853890310017161

21 January 2018

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

15000344

1 reference

Consolidated OpenCitations Corpus – April 2017