(Q44403968)

2 December 2017

title

Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy (English)

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2 December 2017

Tiina Heliö

2

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Markku Laakso

series ordinal

12

object named as

Markku Laakso

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2 December 2017

11

Johanna Kuusisto

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2 December 2017

3

Pertti Jääskeläinen

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2 December 2017

4

Raija Miettinen

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2 December 2017

9

Lauri Toivonen

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2 December 2017

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Maija Kaartinen

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2 December 2017

1

Satu Kärkkäinen

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2 December 2017

8

Eeva Reissell

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2 December 2017

13

Keijo Peuhkurinen

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2 December 2017

5

Petri Tuomainen

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2 December 2017

6

Kari Ylitalo

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2 December 2017

Markku S Nieminen

10

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2 December 2017

publication date

1 December 2004

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European Journal of Heart Failure

2 December 2017

published in

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2 December 2017

volume

6

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2 December 2017

issue

7

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2 December 2017

page(s)

861-868

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Frequency and phenotypes of familial dilated cardiomyopathy.

2 December 2017

cites work

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Desmin mutation responsible for idiopathic dilated cardiomyopathy

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Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy

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Metavinculin mutations alter actin interaction in dilated cardiomyopathy.

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Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban

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The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy

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Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

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Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy

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Titin mutations as the molecular basis for dilated cardiomyopathy

21 January 2018

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Many roads lead to a broken heart: the genetics of dilated cardiomyopathy

21 January 2018

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

21 January 2018

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The molecular genetic basis for hypertrophic cardiomyopathy

21 January 2018

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Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly

21 January 2018

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Cardiac troponin T Arg92Trp mutation and progression from hypertrophic to dilated cardiomyopathy

21 January 2018

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A novel mutation Lys273Glu in the cardiac troponin T gene shows high degree of penetrance and transition from hypertrophic to dilated cardiomyopathy

21 January 2018

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Novel missense mutation in cardiac troponin T gene found in Japanese patient with hypertrophic cardiomyopathy

21 January 2018

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21 January 2018

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

21 January 2018

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A novel missense mutation in the myosin binding protein-C gene is responsible for hypertrophic cardiomyopathy with left ventricular dysfunction and dilation in elderly patients

21 January 2018

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Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy

21 January 2018

1 reference

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Mutations in beta-myosin S2 that cause familial hypertrophic cardiomyopathy (FHC) abolish the interaction with the regulatory domain of myosin-binding protein-C

21 January 2018

1 reference

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A 29 residue region of the sarcomeric myosin rod is necessary for filament formation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2004.04.017

Progression of left ventricular enlargement in patients with hypertrophic cardiomyopathy: incidence and prognostic value.

21 January 2018

1 reference

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Clinicopathologic features of hypertrophic cardiomyopathy managed by cardiac transplantation

21 January 2018

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Genomic organisation, alternative splicing and polymorphisms of the human cardiac troponin T gene

21 January 2018

1 reference

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10.1016/J.EJHEART.2004.04.017

21 January 2018

Identifiers

DOI

1 reference

2 December 2017

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