Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy. (Q44690426)

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scientific article published on 25 October 2008

Language	Label	Description	Also known as
English	Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy.	scientific article published on 25 October 2008

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18953637%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy (English)

1 reference

Europe PubMed Central

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25 December 2019

8

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25 December 2019

Taranjit Singh Rai

1

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25 December 2019

7

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25 December 2019

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Shamim Ahmad

2

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25 December 2019

Ajay Bahl

3

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25 December 2019

Monica Ahuja

4

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25 December 2019

Tarunveer Singh Ahluwalia

5

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25 December 2019

Balvinder Singh

6

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25 December 2019

publication date

25 October 2008

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25 December 2019

Molecular and Cellular Biochemistry

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25 December 2019

321

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25 December 2019

1-2

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25 December 2019

189-196

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25 December 2019

Genotype-phenotype correlations in hypertrophic cardiomyopathy. Insights provided by comparisons of kindreds with distinct and identical beta-myosin heavy chain gene mutations

1 reference

https://api.crossref.org/works/10.1007%2FS11010-008-9932-0

21 January 2018

A p.R870H mutation in the beta-cardiac myosin heavy chain 7 gene causes familial hypertrophic cardiomyopathy in several members of an Indian family

1 reference

https://api.crossref.org/works/10.1007%2FS11010-008-9932-0

21 January 2018

Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

1 reference

https://api.crossref.org/works/10.1007%2FS11010-008-9932-0

21 January 2018

The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18953637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Skeletal muscle expression and abnormal function of beta-myosin in hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18953637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characteristics of the beta myosin heavy chain gene Ala26Val mutation in a Chinese family with hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18953637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18953637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early expression of a malignant phenotype of familial hypertrophic cardiomyopathy associated with a Gly716Arg myosin heavy chain mutation in a Korean family

1 reference

https://pubmed.ncbi.nlm.nih.gov/18953637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A missense mutation in the beta-myosin heavy chain gene in a Japanese patient with hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18953637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18953637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simulations of the myosin II motor reveal a nucleotide-state sensing element that controls the recovery stroke

1 reference

https://pubmed.ncbi.nlm.nih.gov/18953637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence and severity of "benign" mutations in the beta-myosin heavy chain, cardiac troponin T, and alpha-tropomyosin genes in hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18953637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype-phenotype correlation of R870H mutation in hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18953637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18953637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18953637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A myosin missense mutation, not a null allele, causes familial hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18953637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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