17635512

Source:http://linkedlifedata.com/resource/pubmed/id/17635512

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0011155, umls-concept:C0020758, umls-concept:C0220908, umls-concept:C0344329, umls-concept:C0392360, umls-concept:C0441748, umls-concept:C0538672, umls-concept:C0599894, umls-concept:C1180925, umls-concept:C1521840, umls-concept:C1521991
pubmed:issue	4
pubmed:dateCreated	2007-9-14
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0004041
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Transglutaminases, http://linkedlifedata.com/resource/pubmed/chemical/transglutaminase 1
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	0007-0963
pubmed:author	pubmed-author:AuricchioLL, pubmed-author:EspositoGG, pubmed-author:GiordanoLL, pubmed-author:IenoLL, pubmed-author:MessinaFF, pubmed-author:PaparoFF, pubmed-author:PennacchiaWW, pubmed-author:PiccirilloAA, pubmed-author:TadiniGG, pubmed-author:ViolaAA
pubmed:issnType	Print
pubmed:volume	157
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	808-10
pubmed:meshHeading	pubmed-meshheading:17635512-Base Sequence, pubmed-meshheading:17635512-DNA Mutational Analysis, pubmed-meshheading:17635512-Epidermis, pubmed-meshheading:17635512-Humans, pubmed-meshheading:17635512-Ichthyosiform Erythroderma, Congenital, pubmed-meshheading:17635512-Mutation, pubmed-meshheading:17635512-Transglutaminases
pubmed:year	2007
pubmed:articleTitle	Transglutaminase 1 deficiency and corneocyte collapse: an indication for targeted molecular screening in autosomal recessive congenital ichthyosis.
pubmed:publicationType	Letter, Research Support, Non-U.S. Gov't