(Q33312381)

25 July 2017

Noncompaction of the ventricular myocardium is associated with a de novo mutation in the beta-myosin heavy chain gene (English)

1 reference

25 July 2017

Wulf Blankenfeldt

5

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Roger S. Goody

object named as

Roger S Goody

15

0 references

Peter Nürnberg

17

object named as

Peter Nürnberg

1 reference

25 July 2017

Birgit S Budde

1

1 reference

25 July 2017

Priska Binner

2

1 reference

25 July 2017

Stephan Waldmüller

3

1 reference

25 July 2017

Wolfgang Höhne

4

1 reference

25 July 2017

Sabine Hassfeld

6

1 reference

25 July 2017

Jürgen Brömsen

7

1 reference

25 July 2017

Anastassia Dermintzoglou

8

1 reference

25 July 2017

Marcus Wieczorek

9

1 reference

25 July 2017

Erik May

10

1 reference

25 July 2017

Elisabeth Kirst

11

1 reference

25 July 2017

Carmen Selignow

12

1 reference

25 July 2017

Kirsten Rackebrandt

13

1 reference

25 July 2017

Melanie Müller

14

1 reference

25 July 2017

Hans-Peter Vosberg

16

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25 July 2017

Thomas Scheffold

18

1 reference

25 July 2017

language of work or name

English

0 references

publication date

26 December 2007

1 reference

25 July 2017

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25 July 2017

2

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25 July 2017

12

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25 July 2017

e1362

1 reference

Creative Commons Attribution 4.0 International

25 July 2017

start time

26 December 2007

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Genetics of dilated cardiomyopathy

1 reference

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Genetic basis of hypertrophic cardiomyopathy.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Genetics of right ventricular cardiomyopathy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Mutation in myosin heavy chain 6 causes atrial septal defect

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Novel gene locus for autosomal dominant left ventricular noncompaction maps to chromosome 11p15.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Mutations of the beta myosin heavy chain gene in hypertrophic cardiomyopathy: critical functional sites determine prognosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Isolated left ventricular noncompaction: an unclassified cardiomyopathy with severe prognosis in adults

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Developmental patterning of the myocardium

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Three-dimensional structure of myosin subfragment-1: a molecular motor

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Identification of a rare congenital anomaly of the myocardium by two-dimensional echocardiography: persistence of isolated myocardial sinusoids

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Molecular cloning and characterization of human cardiac alpha- and beta-form myosin heavy chain complementary DNA clones. Regulation of expression during development and pressure overload in human atrium

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Isolated noncompaction of left ventricular myocardium. A study of eight cases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

The complete sequence of the human beta-myosin heavy chain gene and a comparative analysis of its product

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Dinucleotide repeat polymorphism at the human cardiac beta-myosin gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies.

21 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001362

Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathy

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001362

Human cardiac myosin heavy chain isoforms in fetal and failing adult atria and ventricles

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2137931

Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene

31 October 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001362

Exclusion of cardiac myosin heavy chain and actin gene involvement in hypertrophic cardiomyopathy of several French families

21 January 2018

1 reference

12 December 2020

1 reference

12 December 2020

Ventricular noncompaction and distal chromosome 5q deletion

1 reference

12 December 2020

Natural history and familial characteristics of isolated left ventricular non-compaction

1 reference

12 December 2020

easyLINKAGE: a PERL script for easy and automated two-/multi-point linkage analyses

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0001362

Identifiers

DOI

1 reference

25 July 2017

0 references

1 reference

25 July 2017

1 reference