21565790

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Subject	Predicate	Object	Context
pubmed-article:21565790	rdf:type	pubmed:Citation	lld:pubmed
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pubmed-article:21565790	lifeskim:mentions	umls-concept:C0205314	lld:lifeskim
pubmed-article:21565790	pubmed:issue	8	lld:pubmed
pubmed-article:21565790	pubmed:dateCreated	2011-8-5	lld:pubmed
pubmed-article:21565790	pubmed:abstractText	Congenital hypothyroidism (CH) associated with goiter or a gland of normal size has been linked to dual oxidase 2 (DUOX2) mutations in the presence of iodide organification defect.	lld:pubmed
pubmed-article:21565790	pubmed:language	eng	lld:pubmed
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pubmed-article:21565790	pubmed:citationSubset	AIM	lld:pubmed
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pubmed-article:21565790	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:21565790	pubmed:month	Aug	lld:pubmed
pubmed-article:21565790	pubmed:issn	1945-7197	lld:pubmed
pubmed-article:21565790	pubmed:author	pubmed-author:PincheraAldoA	lld:pubmed
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pubmed-article:21565790	pubmed:issnType	Electronic	lld:pubmed
pubmed-article:21565790	pubmed:volume	96	lld:pubmed
pubmed-article:21565790	pubmed:owner	NLM	lld:pubmed
pubmed-article:21565790	pubmed:authorsComplete	Y	lld:pubmed
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pubmed-article:21565790	pubmed:meshHeading	pubmed-meshheading:21565790...	lld:pubmed
pubmed-article:21565790	pubmed:year	2011	lld:pubmed
pubmed-article:21565790	pubmed:articleTitle	Identification and functional analysis of novel dual oxidase 2 (DUOX2) mutations in children with congenital or subclinical hypothyroidism.	lld:pubmed
pubmed-article:21565790	pubmed:affiliation	Dipartimento di Endocrinologia, Università di Pisa, Via Paradisa 2, 56124, Cisanello, Pisa, Italy.	lld:pubmed
pubmed-article:21565790	pubmed:publicationType	Journal Article	lld:pubmed
pubmed-article:21565790	pubmed:publicationType	Research Support, Non-U.S. Gov't	lld:pubmed
entrez-gene:50506	entrezgene:pubmed	pubmed-article:21565790	lld:entrezgene
http://linkedlifedata.com/r...	entrezgene:pubmed	pubmed-article:21565790	lld:entrezgene