Nemaline myopathy and non-fatal hypertrophic cardiomyopathy caused by a novel ACTA1 E239K mutation (Q45956684)

From Wikidata

Jump to navigation Jump to search

scientific article published on May 13, 2011

edit

Language	Label	Description	Also known as
English	Nemaline myopathy and non-fatal hypertrophic cardiomyopathy caused by a novel ACTA1 E239K mutation	scientific article published on May 13, 2011

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21570694

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/21570694

title

Nemaline myopathy and non-fatal hypertrophic cardiomyopathy caused by a novel ACTA1 E239K mutation (English)

1 reference

stated in

Crossref

DOI

10.1016/J.JNS.2011.04.022

reference URL

https://api.crossref.org/works/10.1016/J.JNS.2011.04.022

retrieved

2 December 2024

main subject

hypertrophic cardiomyopathy

1 reference

based on heuristic

inferred from title

nemaline myopathy

1 reference

based on heuristic

inferred from title

author name string

Sun-Young Kim

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21570694

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/21570694

Young-Eun Park

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21570694

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/21570694

Hyang-Sook Kim

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21570694

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/21570694

Chang-Hoon Lee

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21570694

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/21570694

Dong Heon Yang

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21570694

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/21570694

Dae-Seong Kim

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21570694

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/21570694

language of work or name

English

1 reference

stated in

National Center for Biotechnology Information

PubMed publication ID

21570694

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21570694

retrieved

2 December 2024

publication date

13 May 2011

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21570694

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/21570694

full work available at URL

https://api.elsevier.com/content/article/PII:S0022510X11002255?httpAccept=text/xml

1 reference

stated in

Crossref

DOI

10.1016/J.JNS.2011.04.022

reference URL

https://api.crossref.org/works/10.1016/J.JNS.2011.04.022

retrieved

2 December 2024

https://api.elsevier.com/content/article/PII:S0022510X11002255?httpAccept=text/plain

1 reference

stated in

Crossref

DOI

10.1016/J.JNS.2011.04.022

reference URL

https://api.crossref.org/works/10.1016/J.JNS.2011.04.022

retrieved

2 December 2024

published in

Journal of the Neurological Sciences

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21570694

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/21570694

volume

307

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21570694

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/21570694

issue

1-2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21570694

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/21570694

page(s)

171-173

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21570694

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/21570694

cites work

Congenital myopathies

series ordinal

1

1 reference

stated in

Crossref

DOI

10.1016/J.JNS.2011.04.022

reference URL

https://api.crossref.org/works/10.1016/J.JNS.2011.04.022

retrieved

2 December 2024

NEMALINE MYOPATHY

series ordinal

2

1 reference

stated in

Crossref

DOI

10.1016/J.JNS.2011.04.022

reference URL

https://api.crossref.org/works/10.1016/J.JNS.2011.04.022

retrieved

2 December 2024

Congenital myopathies--a comprehensive update of recent advancements

series ordinal

3

1 reference

stated in

Crossref

DOI

10.1016/J.JNS.2011.04.022

reference URL

https://api.crossref.org/works/10.1016/J.JNS.2011.04.022

retrieved

2 December 2024

Defining alpha-skeletal and alpha-cardiac actin expression in human heart and skeletal muscle explains the absence of cardiac involvement in ACTA1 nemaline myopathy

series ordinal

4

1 reference

stated in

Crossref

DOI

10.1016/J.JNS.2011.04.022

reference URL

https://api.crossref.org/works/10.1016/J.JNS.2011.04.022

retrieved

2 December 2024

An infant with congenital nemaline myopathy and hypertrophic cardiomyopathy

series ordinal

5

1 reference

stated in

Crossref

DOI

10.1016/J.JNS.2011.04.022

reference URL

https://api.crossref.org/works/10.1016/J.JNS.2011.04.022

retrieved

2 December 2024

Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation

series ordinal

6

1 reference

stated in

Crossref

DOI

10.1016/J.JNS.2011.04.022

reference URL

https://api.crossref.org/works/10.1016/J.JNS.2011.04.022

retrieved

2 December 2024

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy

series ordinal

7

1 reference

stated in

Crossref

DOI

10.1016/J.JNS.2011.04.022

reference URL

https://api.crossref.org/works/10.1016/J.JNS.2011.04.022

retrieved

2 December 2024

Nemaline myopathy and cardiomyopathy

series ordinal

8

1 reference

stated in

Crossref

DOI

10.1016/J.JNS.2011.04.022

reference URL

https://api.crossref.org/works/10.1016/J.JNS.2011.04.022

retrieved

2 December 2024

Nemaline myopathy associated with hypertrophic cardiomyopathy

series ordinal

9

1 reference

stated in

Crossref

DOI

10.1016/J.JNS.2011.04.022

reference URL

https://api.crossref.org/works/10.1016/J.JNS.2011.04.022

retrieved

2 December 2024

Myopathy mutations in alpha-skeletal-muscle actin cause a range of molecular defects.

series ordinal

10

1 reference

stated in

Crossref

DOI

10.1016/J.JNS.2011.04.022

reference URL

https://api.crossref.org/works/10.1016/J.JNS.2011.04.022

retrieved

2 December 2024

Identifiers

DOI

10.1016/J.JNS.2011.04.022

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21570694

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/21570694

PubMed publication ID

21570694

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21570694

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/21570694

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q45956684&oldid=2282499797"