Wikidata

(Q43073543)

English

Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease

scientific article published in September 2004

In more languages

Statements

title
Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease (English)
1 reference
stated in
Europe PubMed Central
PMCID
1735891
retrieved
13 November 2017
author name string
S M Reamon-Buettner
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1735891
retrieved
13 November 2017
J Borlak
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1735891
retrieved
13 November 2017
publication date
1 September 2004
1 reference
stated in
Europe PubMed Central
PMCID
1735891
retrieved
13 November 2017
volume
41
1 reference
stated in
Europe PubMed Central
PMCID
1735891
retrieved
13 November 2017
issue
9
1 reference
stated in
Europe PubMed Central
PMCID
1735891
retrieved
13 November 2017
page(s)
684-690
1 reference
stated in
Europe PubMed Central
PMCID
1735891
retrieved
13 November 2017

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