(Q34372769)

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High prevalence of Arginine to Glutamine substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians

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Europe PubMed Central

PubMed publication ID

1 August 2017

High prevalence of Arginine to Glutamine substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

hypertrophic cardiomyopathy

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based on heuristic

inferred from title

Kumarasamy Thangaraj

6

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Europe PubMed Central

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1 August 2017

author name string

Deepa Selvi Rani

1

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Europe PubMed Central

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1 August 2017

Pratibha Nallari

2

1 reference

Europe PubMed Central

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1 August 2017

Singh Priyamvada

3

1 reference

Europe PubMed Central

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1 August 2017

Calambur Narasimhan

4

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Europe PubMed Central

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1 August 2017

Lalji Singh

5

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Europe PubMed Central

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1 August 2017

publication date

10 August 2012

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Europe PubMed Central

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1 August 2017

BMC Medical Genetics

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Europe PubMed Central

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1 August 2017

13

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Europe PubMed Central

PubMed publication ID

1 August 2017

69

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Europe PubMed Central

PubMed publication ID

1 August 2017

Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495047

6 July 2018

A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495047

6 July 2018

MYBPC3 gene variations in hypertrophic cardiomyopathy patients in India

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495047

6 July 2018

A second generation human haplotype map of over 3.1 million SNPs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495047

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495047

6 July 2018

The relationship between synonymous codon usage and protein structure in Escherichia coli and Homo sapiens.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495047

6 July 2018

Expression patterns and gene distribution in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495047

6 July 2018

Hypertrophic cardiomyopathy: a systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495047

6 July 2018

Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495047

6 July 2018

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495047

6 July 2018

Isolation and characterization of the human cardiac troponin I gene (TNNI3)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495047

6 July 2018

Codon catalog usage and the genome hypothesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495047

6 July 2018

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

1 reference

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6 July 2018

Splice junctions, branch point sites, and exons: sequence statistics, identification, and applications to genome project

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3495047

6 July 2018

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-69

21 January 2018

Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-69

21 January 2018

CAG repeat variation in the mtDNA polymerase γ is not associated with oligoasthenozoospermia

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-69

21 January 2018

Identifiers

10.1186/1471-2350-13-69

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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