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15557537
Source:
http://linkedlifedata.com/resource/pubmed/id/15557537
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Inference
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0019202
,
umls-concept:C0019904
,
umls-concept:C0026882
,
umls-concept:C0205314
,
umls-concept:C0449450
,
umls-concept:C0679622
pubmed:issue
10
pubmed:dateCreated
2004-11-23
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Adenosine Triphosphatases
,
http://linkedlifedata.com/resource/pubmed/chemical/Cation Transport Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/Codon
,
http://linkedlifedata.com/resource/pubmed/chemical/Wilson disease protein
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1526-632X
pubmed:author
pubmed-author:BurtonE AEA
,
pubmed-author:DaltonAA
,
pubmed-author:PendleburyS TST
,
pubmed-author:RothwellP MPM
pubmed:issnType
Electronic
pubmed:day
23
pubmed:volume
63
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1982-3
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15557537-Adenosine Triphosphatases
,
pubmed-meshheading:15557537-Amino Acid Substitution
,
pubmed-meshheading:15557537-Basal Ganglia
,
pubmed-meshheading:15557537-Brain Ischemia
,
pubmed-meshheading:15557537-Cation Transport Proteins
,
pubmed-meshheading:15557537-Codon
,
pubmed-meshheading:15557537-Dysarthria
,
pubmed-meshheading:15557537-Gait Disorders, Neurologic
,
pubmed-meshheading:15557537-Hepatolenticular Degeneration
,
pubmed-meshheading:15557537-Homozygote
,
pubmed-meshheading:15557537-Humans
,
pubmed-meshheading:15557537-Mesencephalon
,
pubmed-meshheading:15557537-Mutation, Missense
,
pubmed-meshheading:15557537-Point Mutation
,
pubmed-meshheading:15557537-Tomography, X-Ray Computed
pubmed:year
2004
pubmed:articleTitle
Strokelike presentation of Wilson disease with homozygosity for a novel T766R mutation.
pubmed:affiliation
Departments of General Medicine, University of Oxford, UK.
pubmed:publicationType
Journal Article
,
Case Reports