16965439

Source:http://linkedlifedata.com/resource/pubmed/id/16965439

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0019425, umls-concept:C0026882, umls-concept:C0079474, umls-concept:C0205198, umls-concept:C1314792, umls-concept:C1413592, umls-concept:C1533148
pubmed:issue	4
pubmed:dateCreated	2006-9-12
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0004041
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Collagen Type VII
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	0007-0963
pubmed:author	pubmed-author:FujiwaraHH, pubmed-author:ItoMM, pubmed-author:KariyaNN, pubmed-author:ShibuyaMM, pubmed-author:ShimomuraYY, pubmed-author:SuzukiSS, pubmed-author:YamamotoYY
pubmed:issnType	Print
pubmed:volume	155
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	838-40
pubmed:meshHeading	pubmed-meshheading:16965439-Base Sequence, pubmed-meshheading:16965439-Collagen Type VII, pubmed-meshheading:16965439-DNA Mutational Analysis, pubmed-meshheading:16965439-Epidermolysis Bullosa Dystrophica, pubmed-meshheading:16965439-Female, pubmed-meshheading:16965439-Heterozygote, pubmed-meshheading:16965439-Humans, pubmed-meshheading:16965439-Infant, Newborn, pubmed-meshheading:16965439-Mutation
pubmed:year	2006
pubmed:articleTitle	A case of recessive dystrophic epidermolysis bullosa caused by compound heterozygous mutations in the COL7A1 gene.
pubmed:affiliation	Department of Dermatology, Niigata University School of Medicine, Asahimachi-dori, Niigata 951-8510, Japan.
pubmed:publicationType	Journal Article, Case Reports