18070134

Source:http://linkedlifedata.com/resource/pubmed/id/18070134

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0013720, umls-concept:C0020792, umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0031437, umls-concept:C0205314, umls-concept:C0332307, umls-concept:C0679622, umls-concept:C1336624, umls-concept:C1801960, umls-concept:C2697932
pubmed:issue	3
pubmed:dateCreated	2008-2-13
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0253664
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/COL3A1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Collagen Type III, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Transforming Growth..., http://linkedlifedata.com/resource/pubmed/chemical/TGF-beta type I receptor
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	1399-0004
pubmed:author	pubmed-author:BarlatiSS, pubmed-author:ColomboCC, pubmed-author:DreraBB, pubmed-author:TadiniGG
pubmed:issnType	Electronic
pubmed:volume	73
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	290-3
pubmed:meshHeading	pubmed-meshheading:18070134-Abnormalities, Multiple, pubmed-meshheading:18070134-Amino Acid Sequence, pubmed-meshheading:18070134-Aneurysm, pubmed-meshheading:18070134-Base Sequence, pubmed-meshheading:18070134-Collagen Type III, pubmed-meshheading:18070134-DNA Mutational Analysis, pubmed-meshheading:18070134-Ehlers-Danlos Syndrome, pubmed-meshheading:18070134-Female, pubmed-meshheading:18070134-Humans, pubmed-meshheading:18070134-Male, pubmed-meshheading:18070134-Middle Aged, pubmed-meshheading:18070134-Molecular Sequence Data, pubmed-meshheading:18070134-Mutation, pubmed-meshheading:18070134-Pedigree, pubmed-meshheading:18070134-Phenotype, pubmed-meshheading:18070134-Protein-Serine-Threonine Kinases, pubmed-meshheading:18070134-Receptors, Transforming Growth Factor beta, pubmed-meshheading:18070134-Syndrome
pubmed:year	2008
pubmed:articleTitle	Identification of a novel TGFBR1 mutation in a Loeys-Dietz syndrome type II patient with vascular Ehlers-Danlos syndrome phenotype.
pubmed:publicationType	Letter, Case Reports, Research Support, Non-U.S. Gov't