The cardiac beta-myosin heavy chain gene is not the predominant gene for hypertrophic cardiomyopathy in the Finnish population. (Q52906642)

9 May 2018

title

The cardiac beta-myosin heavy chain gene is not the predominant gene for hypertrophic cardiomyopathy in the Finnish population. (English)

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9 May 2018

hypertrophic cardiomyopathy

main subject

Finland

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5

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Markku Laakso

8

object named as

Laakso M

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Jääskeläinen P

1

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Soranta M

2

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Miettinen R

3

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Saarinen L

4

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Silvennoinen K

6

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Tikanoja T

7

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Kuusisto J

9

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language of work or name

English

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publication date

1 November 1998

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9 May 2018

Journal of the American College of Cardiology

published in

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volume

32

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issue

6

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page(s)

1709-1716

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Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (1).

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (2).

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Detection of a new mutation in the beta-myosin heavy chain gene in an individual with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Novel missense mutation in alpha-tropomyosin gene found in Japanese patients with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Recent advances in the molecular genetics of hypertrophic cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Clinical implications of hypertrophic cardiomyopathy associated with mutations in the alpha-tropomyosin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

The management of hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Clinical course and prognosis of hypertrophic cardiomyopathy in an outpatient population

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Experience from clinical genetics in hypertrophic cardiomyopathy: proposal for new diagnostic criteria in adult members of affected families

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Age and body surface area related normal upper and lower limits of M mode echocardiographic measurements and left ventricular volume and mass from infancy to early adulthood

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

The complete sequence of the human beta-myosin heavy chain gene and a comparative analysis of its product

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Complete sequence and organization of the human cardiac beta-myosin heavy chain gene

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Direct sequencing from low-melt agarose with Sequenase.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Exclusion of cardiac myosin heavy chain and actin gene involvement in hypertrophic cardiomyopathy of several French families

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

The LPL gene in individuals with familial combined hyperlipidemia and decreased LPL activity

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Polymorphism in red photopigment underlies variation in colour matching

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Selective expression of human X chromosome-linked green opsin genes

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

Insulin receptor substrate-1 variants in non-insulin-dependent diabetes

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900448-3

7 January 2021

10.1016/S0735-1097(98)00448-3

Identifiers

DOI

1 reference

9 May 2018

PubMed ID

9822100

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9 May 2018