Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2011-8-5
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.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1945-7197
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
96
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
E1335-9
pubmed:meshHeading
pubmed:year
2011
pubmed:articleTitle
Identification and functional analysis of novel dual oxidase 2 (DUOX2) mutations in children with congenital or subclinical hypothyroidism.
pubmed:affiliation
Dipartimento di Endocrinologia, Università di Pisa, Via Paradisa 2, 56124, Cisanello, Pisa, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't