E101K and M123V alpha-cardiac actin gene mutations are not associated with cardiomyopathy in Iranian population.

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E101K and M123V alpha-cardiac actin gene mutations are not associated with cardiomyopathy in Iranian population.

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年學術文章

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2015年學術文章

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E101K and M123V alpha-cardiac ...... yopathy in Iranian population.

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E101K and M123V alpha-cardiac ...... yopathy in Iranian population.

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Item

label

E101K and M123V alpha-cardiac ...... yopathy in Iranian population.

@ast

E101K and M123V alpha-cardiac ...... yopathy in Iranian population.

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prefLabel

E101K and M123V alpha-cardiac ...... yopathy in Iranian population.

@ast

E101K and M123V alpha-cardiac ...... yopathy in Iranian population.

@en

P1476

E101K and M123V alpha-cardiac ...... yopathy in Iranian population.

@en

P2093

Asiyeh Jebelli

http://www.w3.org/2001/XMLSchema#string

Eshrat Beyranvand

http://www.w3.org/2001/XMLSchema#string

Hakimeh Sadeghian

http://www.w3.org/2001/XMLSchema#string

Mehrdad Behmanesh

http://www.w3.org/2001/XMLSchema#string

Mohammad Ali Boroumand

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P2860

Defining alpha-skeletal and alpha-cardiac actin expression in human heart and skeletal muscle explains the absence of cardiac involvement in ACTA1 nemaline myopathy

Alpha-cardiac actin mutations produce atrial septal defects

Reduced ACTC1 expression might play a role in the onset of congenital heart disease by inducing cardiomyocyte apoptosis

Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects

Functional consequences of a mutation in an expressed human alpha-cardiac actin at a site implicated in familial hypertrophic cardiomyopathy

Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy

The functional importance of multiple actin isoforms

Mutations in sarcomere protein genes in left ventricular noncompaction

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.

Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation.

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289-294

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P31

scholarly article

P433

http://www.w3.org/2001/XMLSchema#string

P478

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P577

2015-09-01T00:00:00Z

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P698

26715934

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P932

4680077

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