17635506

Source:http://linkedlifedata.com/resource/pubmed/id/17635506

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0022595, umls-concept:C0026882, umls-concept:C0034897, umls-concept:C0079298, umls-concept:C0333275, umls-concept:C0860439, umls-concept:C1412638, umls-concept:C1556094
pubmed:issue	3
pubmed:dateCreated	2007-8-16
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0004041
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Keratin-14
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	0007-0963
pubmed:author	pubmed-author:HamadaTT, pubmed-author:HashimotoTT, pubmed-author:ImayamaSS, pubmed-author:IshiiNN, pubmed-author:KarashimaTT, pubmed-author:KawanoYY, pubmed-author:McGrathJ AJA, pubmed-author:ShimadaHH, pubmed-author:YasumotoSS
pubmed:issnType	Print
pubmed:volume	157
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	605-8
pubmed:dateRevised	2008-11-21
pubmed:meshHeading	pubmed-meshheading:17635506-Adult, pubmed-meshheading:17635506-Darier Disease, pubmed-meshheading:17635506-Diagnosis, Differential, pubmed-meshheading:17635506-Epidermolysis Bullosa Simplex, pubmed-meshheading:17635506-Female, pubmed-meshheading:17635506-Humans, pubmed-meshheading:17635506-Keratin-14, pubmed-meshheading:17635506-Pedigree, pubmed-meshheading:17635506-Pigmentation Disorders, pubmed-meshheading:17635506-Treatment Outcome
pubmed:year	2007
pubmed:articleTitle	Recurrent p.N767S mutation in the ATP2A2 gene in a Japanese family with haemorrhagic Darier disease clinically mimicking epidermolysis bullosa simplex with mottled pigmentation.
pubmed:affiliation	Department of Dermatology, Kurume University School of Medicine, 67 Asahimachi, Kurume 830-0011, Japan. hamataka@med.kurume-u.ac.jp
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't