3663407

Source:http://linkedlifedata.com/resource/pubmed/id/3663407

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007320, umls-concept:C0014527, umls-concept:C0085973, umls-concept:C0332307, umls-concept:C0441748, umls-concept:C2607943, umls-concept:C2926606
pubmed:issue	4
pubmed:dateCreated	1987-11-25
pubmed:language	jpn
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0215224
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0029-0831
pubmed:author	pubmed-author:AraiYY, pubmed-author:InoharaRR, pubmed-author:IshizakiAA, pubmed-author:KawaiMM, pubmed-author:MorimatsuYY, pubmed-author:SakamotoKK, pubmed-author:SatohJJ, pubmed-author:ShinoharaTT, pubmed-author:ShinozakiMM
pubmed:issnType	Print
pubmed:volume	19
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	322-7
pubmed:dateRevised	2008-12-25
pubmed:meshHeading	pubmed-meshheading:3663407-Brain, pubmed-meshheading:3663407-Child, pubmed-meshheading:3663407-Epidermolysis Bullosa, pubmed-meshheading:3663407-Genes, Recessive, pubmed-meshheading:3663407-Humans, pubmed-meshheading:3663407-Male, pubmed-meshheading:3663407-Skin, pubmed-meshheading:3663407-Spinal Cord, pubmed-meshheading:3663407-Vitamin B Deficiency
pubmed:year	1987
pubmed:articleTitle	[Neuropathological findings on epidermolysis bullosa hereditaria (autosomal recessive dystrophic type)--a case report].
pubmed:publicationType	Journal Article, English Abstract, Case Reports