11415848

Source:http://linkedlifedata.com/resource/pubmed/id/11415848

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0010308, umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0205314, umls-concept:C0205355, umls-concept:C0679622, umls-concept:C1364508
pubmed:issue	1
pubmed:dateCreated	2001-6-20
pubmed:abstractText	It is suggested that iodide organification defects account for 10% of all cases with congenital hypothyroidism (CH). One candidate gene for these defects is the thyroid peroxidase (TPO) gene.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9423848
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, http://linkedlifedata.com/resource/pubmed/chemical/Iodide Peroxidase, http://linkedlifedata.com/resource/pubmed/chemical/Thyroglobulin, http://linkedlifedata.com/resource/pubmed/chemical/Thyrotropin, http://linkedlifedata.com/resource/pubmed/chemical/Thyroxine
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	0804-4643
pubmed:author	pubmed-author:AmbruggerPP, pubmed-author:BiebermannHH, pubmed-author:GrütersAA, pubmed-author:LeitnerCC, pubmed-author:StoevaII, pubmed-author:TorresaniTT
pubmed:issnType	Print
pubmed:volume	145
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	19-24
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:11415848-Congenital Hypothyroidism, pubmed-meshheading:11415848-DNA, pubmed-meshheading:11415848-Electrophoresis, Agar Gel, pubmed-meshheading:11415848-Female, pubmed-meshheading:11415848-Humans, pubmed-meshheading:11415848-Hypothyroidism, pubmed-meshheading:11415848-Infant, pubmed-meshheading:11415848-Iodide Peroxidase, pubmed-meshheading:11415848-Male, pubmed-meshheading:11415848-Mutation, Missense, pubmed-meshheading:11415848-Pedigree, pubmed-meshheading:11415848-Point Mutation, pubmed-meshheading:11415848-Polymerase Chain Reaction, pubmed-meshheading:11415848-Polymorphism, Single-Stranded Conformational, pubmed-meshheading:11415848-Sequence Analysis, DNA, pubmed-meshheading:11415848-Thyroglobulin, pubmed-meshheading:11415848-Thyrotropin, pubmed-meshheading:11415848-Thyroxine
pubmed:year	2001
pubmed:articleTitle	Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidism.
pubmed:affiliation	Otto Heubner Zentrum für Kinder- und Jugendmedizin, Pädiatrische Endokrinologie, CVK, Humboldt University, Berlin, Germany.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't