(Q71793877)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581410%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

title

Identification of a novel Ala797Thr mutation in exon 21 of the beta-myosin heavy chain gene in hypertrophic cardiomyopathy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581410%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

Identification of a novel Ala797Thr mutation in exon 21 of the β-myosin heavy chain gene in hypertrophic cardiomyopathy (English)

1 reference

https://api.crossref.org/works/10.1002/HUMU.1380060219

hypertrophic cardiomyopathy

22 May 2024

main subject

1 reference

J. C. Moolman

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7581410

22 May 2024

P. A. Brink

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7581410

22 May 2024

V. A. Corfield

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7581410

22 May 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7581410

22 May 2024

publication date

1 January 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581410%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

21 October 2019

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fhumu.1380060219

1 reference

https://api.crossref.org/works/10.1002/HUMU.1380060219

https://onlinelibrary.wiley.com/doi/full/10.1002/humu.1380060219

22 May 2024

1 reference

https://api.crossref.org/works/10.1002/HUMU.1380060219

22 May 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581410%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

volume

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581410%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581410%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

page(s)

197-198

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581410%20AND%20SRC:MED&resulttype=core&format=json

Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11

21 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060219

7 January 2021

Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060219

7 January 2021

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/10.1002%2FHUMU.1380060219

7 January 2021

Localization of gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse US population

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060219

7 January 2021

Genetics of familial hypertrophic cardiomyopathy Results and strategies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060219

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060219

7 January 2021

Identification of a new missense mutation at Arg403, a CpG mutation hotspot, in exon 13 of the beta-myosin heavy chain gene in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060219

7 January 2021

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060219

7 January 2021

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060219

7 January 2021

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060219

7 January 2021

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581410%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference