Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
17
pubmed:dateCreated
1992-11-25
pubmed:abstractText
To identify a possible gene defect in a large kindred with atypical Creutzfeldt-Jakob disease (CJD).
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0098-7484
pubmed:author
pubmed:issnType
Print
pubmed:day
4
pubmed:volume
268
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2413-5
pubmed:dateRevised
2010-3-24
pubmed:meshHeading
pubmed:year
1992
pubmed:articleTitle
Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsy.
pubmed:affiliation
Department of Neurology, Creighton University, Omaha, Neb 68131-2197.
pubmed:publicationType
Journal Article, Case Reports, Research Support, Non-U.S. Gov't