11709001

Source:http://linkedlifedata.com/resource/pubmed/id/11709001

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0012634, umls-concept:C0026882, umls-concept:C0332281, umls-concept:C1418941
pubmed:issue	11
pubmed:dateCreated	2001-11-15
pubmed:abstractText	Gerstmann-Sträussler-Scheinker disease is a rare form of prion disease.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/P30 AG 10133
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0372436
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Prions
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	0003-9942
pubmed:author	pubmed-author:BrownPP, pubmed-author:CernevakovaLL, pubmed-author:DlouhyS RSR, pubmed-author:GhettiBB, pubmed-author:KakulasB ABA, pubmed-author:PanegyresP KPK, pubmed-author:PiccardoPP, pubmed-author:ToufexisKK
pubmed:issnType	Print
pubmed:volume	58
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1899-902
pubmed:dateRevised	2007-11-14
pubmed:meshHeading	pubmed-meshheading:11709001-Base Sequence, pubmed-meshheading:11709001-Brain, pubmed-meshheading:11709001-Gerstmann-Straussler-Scheinker Disease, pubmed-meshheading:11709001-Humans, pubmed-meshheading:11709001-Immunohistochemistry, pubmed-meshheading:11709001-Male, pubmed-meshheading:11709001-Middle Aged, pubmed-meshheading:11709001-Molecular Sequence Data, pubmed-meshheading:11709001-Mutation, pubmed-meshheading:11709001-Prions
pubmed:year	2001
pubmed:articleTitle	A new PRNP mutation (G131V) associated with Gerstmann-Sträussler-Scheinker disease.
pubmed:affiliation	Department of Neuropathology, Royal Perth Hospital, Wellington Street, Perth, Western Australia 6000. peter.panegyres@rph.health.wa.gov.au
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S., Case Reports, Research Support, Non-U.S. Gov't