8956047

Source:http://linkedlifedata.com/resource/pubmed/id/8956047

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017337, umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0043208, umls-concept:C0544512, umls-concept:C1416865, umls-concept:C1556094
pubmed:issue	4
pubmed:dateCreated	1997-3-28
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9215429
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Lipase
pubmed:status	MEDLINE
pubmed:issn	1059-7794
pubmed:author	pubmed-author:FujitaTT, pubmed-author:FujiyamaJJ, pubmed-author:KuriyamaMM, pubmed-author:NagataKK, pubmed-author:NakagawaHH, pubmed-author:OsameMM, pubmed-author:SakurabaHH
pubmed:issnType	Print
pubmed:volume	8
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	377-80
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:8956047-Anemia, pubmed-meshheading:8956047-Cells, Cultured, pubmed-meshheading:8956047-Consanguinity, pubmed-meshheading:8956047-Fatal Outcome, pubmed-meshheading:8956047-Female, pubmed-meshheading:8956047-Fibroblasts, pubmed-meshheading:8956047-Genotype, pubmed-meshheading:8956047-Humans, pubmed-meshheading:8956047-Infant, pubmed-meshheading:8956047-Japan, pubmed-meshheading:8956047-Lipase, pubmed-meshheading:8956047-Liver Failure, pubmed-meshheading:8956047-Lysosomes, pubmed-meshheading:8956047-Male, pubmed-meshheading:8956047-Mutation, pubmed-meshheading:8956047-Phenotype, pubmed-meshheading:8956047-Skin, pubmed-meshheading:8956047-Wolman Disease
pubmed:year	1996
pubmed:articleTitle	A new mutation (LIPA Tyr22X) of lysosomal acid lipase gene in a Japanese patient with Wolman disease.
pubmed:affiliation	Third Department of Internal Medicine, Kagoshima University, School of Medicine, Fukui, Japan.
pubmed:publicationType	Journal Article, Case Reports