rdf:type |
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lifeskim:mentions |
|
pubmed:issue |
21
|
pubmed:dateCreated |
2000-5-25
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pubmed:abstractText |
Mutations in the parkin gene have recently been identified in patients with early-onset Parkinson's disease, but the frequency of the mutations and the associated phenotype have not been assessed in a large series of patients.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
AIM
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pubmed:chemical |
|
pubmed:status |
MEDLINE
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pubmed:month |
May
|
pubmed:issn |
0028-4793
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pubmed:author |
pubmed-author:AgidYY,
pubmed-author:BonifatiVV,
pubmed-author:BriceAA,
pubmed-author:DürrAA,
pubmed-author:De MicheleGG,
pubmed-author:DenèflePP,
pubmed-author:European Consortium on Genetic Susceptibility in Parkinson's Disease,
pubmed-author:French Parkinson's Disease Genetics Study Group,
pubmed-author:GasserTT,
pubmed-author:HarhangiB SBS,
pubmed-author:LückingC BCB,
pubmed-author:MeczLL,
pubmed-author:VaughanJJ,
pubmed-author:WinnR HRH
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pubmed:issnType |
Print
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pubmed:day |
25
|
pubmed:volume |
342
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
1560-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10824074-Adolescent,
pubmed-meshheading:10824074-Adult,
pubmed-meshheading:10824074-Age of Onset,
pubmed-meshheading:10824074-Base Sequence,
pubmed-meshheading:10824074-Child,
pubmed-meshheading:10824074-Exons,
pubmed-meshheading:10824074-Female,
pubmed-meshheading:10824074-Genotype,
pubmed-meshheading:10824074-Humans,
pubmed-meshheading:10824074-Ligases,
pubmed-meshheading:10824074-Male,
pubmed-meshheading:10824074-Middle Aged,
pubmed-meshheading:10824074-Mutation,
pubmed-meshheading:10824074-Parkinsonian Disorders,
pubmed-meshheading:10824074-Phenotype,
pubmed-meshheading:10824074-Point Mutation,
pubmed-meshheading:10824074-Polymerase Chain Reaction,
pubmed-meshheading:10824074-Proteins,
pubmed-meshheading:10824074-Sequence Deletion,
pubmed-meshheading:10824074-Ubiquitin-Protein Ligases
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pubmed:year |
2000
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pubmed:articleTitle |
Association between early-onset Parkinson's disease and mutations in the parkin gene.
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pubmed:affiliation |
INSERM Unité 289, Hôpital de la Salpêtrière, Paris.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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