(Q41511752)

1 October 2017

Short communication: the cardiac myosin binding protein C Arg502Trp mutation: a common cause of hypertrophic cardiomyopathy (English)

1 reference

1 October 2017

Carolyn Y Ho

5

0 references

Heidi L. Rehm

object named as

Heidi L Rehm

16

0 references

Julia Wynn

7

object named as

Julia Wynn

1 reference

1 October 2017

12

Barbara McDonough

1 reference

1 October 2017

14

J G Seidman

1 reference

1 October 2017

15

Christine E Seidman

1 reference

1 October 2017

11

Joshua Gorham

1 reference

1 October 2017

8

Melanie Care

1 reference

1 October 2017

Adam J Saltzman

1

1 reference

1 October 2017

Debora Mancini-DiNardo

2

1 reference

1 October 2017

Chumei Li

3

1 reference

1 October 2017

Wendy K Chung

4

1 reference

1 October 2017

Stephanie Hurst

6

1 reference

1 October 2017

Robert M Hamilton

9

1 reference

1 October 2017

Gregor W Seidman

10

1 reference

1 October 2017

Elizabeth Sparks

13

1 reference

1 October 2017

8 April 2010

1 reference

1 October 2017

1 reference

1 October 2017

106

1 reference

1 October 2017

9

1 reference

1 October 2017

1549-1552

1 reference

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893345

Shared genetic causes of cardiac hypertrophy in children and adults

10 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893345

Classical sickle beta-globin haplotypes exhibit a high degree of long-range haplotype similarity in African and Afro-Caribbean populations

10 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893345

Single-gene mutations and increased left ventricular wall thickness in the community: the Framingham Heart Study

10 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893345

Mutagenesis at methylated CpG sequences.

10 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893345

The genetic basis for cardiac remodeling

10 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893345

Myosin binding protein C: structural abnormalities in familial hypertrophic cardiomyopathy

10 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893345

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

10 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893345

The Genetic Basis for Cardiomyopathy

10 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893345

Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy

10 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893345

The management of hypertrophic cardiomyopathy

10 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893345

Two cases of severe neonatal hypertrophic cardiomyopathy caused by compound heterozygous mutations in the MYBPC3 gene

10 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893345

Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893345

Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893345

The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893345

Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland

19 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20378854

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1161/CIRCRESAHA.109.216291

1 reference

1 October 2017

1 reference

1 October 2017

PubMed publication ID

20378854

1 reference