9266030

Source:http://linkedlifedata.com/resource/pubmed/id/9266030

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0022564, umls-concept:C0023401, umls-concept:C0026882, umls-concept:C0033382, umls-concept:C0079298, umls-concept:C0332307
pubmed:issue	8
pubmed:dateCreated	1997-9-25
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8000462
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Keratins
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	0340-3696
pubmed:author	pubmed-author:FunayamaMM, pubmed-author:HashimotoII, pubmed-author:HosokawaMM, pubmed-author:MenaBB, pubmed-author:MiyazawaTT, pubmed-author:NomuraKK, pubmed-author:SawamuraDD, pubmed-author:TamaiKK, pubmed-author:UmekiKK
pubmed:issnType	Print
pubmed:volume	289
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	493-5
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:9266030-Amino Acid Sequence, pubmed-meshheading:9266030-Child, Preschool, pubmed-meshheading:9266030-Epidermolysis Bullosa Simplex, pubmed-meshheading:9266030-Female, pubmed-meshheading:9266030-Humans, pubmed-meshheading:9266030-Keratins, pubmed-meshheading:9266030-Molecular Sequence Data, pubmed-meshheading:9266030-Phenotype, pubmed-meshheading:9266030-Point Mutation
pubmed:year	1997
pubmed:articleTitle	A keratin K5 mutation (Leu 463-->Pro) in a family with the Weber-Cockayne type of epidermolysis bullosa simplex.
pubmed:affiliation	Department of Dermatology, Hirosaki University School of Medicine, Japan.
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't