9288112

Source:http://linkedlifedata.com/resource/pubmed/id/9288112

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0010308, umls-concept:C0026882, umls-concept:C0597484, umls-concept:C1314792
pubmed:issue	1
pubmed:dateCreated	1997-10-2
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/9288112-9171822
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9216904
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Symporters, http://linkedlifedata.com/resource/pubmed/chemical/sodium-iodide symporter
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	1061-4036
pubmed:author	pubmed-author:FujiwaraHH
pubmed:issnType	Print
pubmed:volume	17
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	122
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:9288112-Amino Acid Sequence, pubmed-meshheading:9288112-Base Sequence, pubmed-meshheading:9288112-Carrier Proteins, pubmed-meshheading:9288112-Consensus Sequence, pubmed-meshheading:9288112-Humans, pubmed-meshheading:9288112-Hypothyroidism, pubmed-meshheading:9288112-Introns, pubmed-meshheading:9288112-Membrane Proteins, pubmed-meshheading:9288112-Molecular Sequence Data, pubmed-meshheading:9288112-Mutation, pubmed-meshheading:9288112-Symporters
pubmed:year	1997
pubmed:articleTitle	Congenital hypothyroidism caused by a mutation in the Na+/l-symporter.
pubmed:publicationType	Published Erratum