12529802

Source:http://linkedlifedata.com/resource/pubmed/id/12529802

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0162534, umls-concept:C0205322, umls-concept:C0439660, umls-concept:C1457887
pubmed:issue	12
pubmed:dateCreated	2003-1-16
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0423161
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Leucine, http://linkedlifedata.com/resource/pubmed/chemical/Prions, http://linkedlifedata.com/resource/pubmed/chemical/Proline
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	0340-5354
pubmed:author	pubmed-author:MizusawaHidehiroH, pubmed-author:ShiraishiAtsushiA, pubmed-author:YamadaMasahitoM
pubmed:issnType	Print
pubmed:volume	249
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1740-1
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:12529802-Female, pubmed-meshheading:12529802-Humans, pubmed-meshheading:12529802-Leucine, pubmed-meshheading:12529802-Male, pubmed-meshheading:12529802-Middle Aged, pubmed-meshheading:12529802-Mutation, pubmed-meshheading:12529802-Pedigree, pubmed-meshheading:12529802-Prion Diseases, pubmed-meshheading:12529802-Prions, pubmed-meshheading:12529802-Proline
pubmed:year	2002
pubmed:articleTitle	Early and persistent sensory-psychiatric symptoms in an inherited prion disease with a PrP P105L mutation.
pubmed:publicationType	Letter, Case Reports, Research Support, Non-U.S. Gov't