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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2005-7-12
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pubmed:abstractText |
To assess the prevalence, nature, and associated phenotypes of PINK1 gene mutations in a large series of patients with early-onset (<50 years) parkinsonism.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1526-632X
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pubmed:author |
pubmed-author:AbbruzzeseGG,
pubmed-author:AntoniniAA,
pubmed-author:BarbosaEE,
pubmed-author:BonifatiVV,
pubmed-author:BreedveldG JGJ,
pubmed-author:ChienH FHF,
pubmed-author:Dalla LiberaAA,
pubmed-author:De GaetanoAA,
pubmed-author:De MariMM,
pubmed-author:De PandisFF,
pubmed-author:FabbriniGG,
pubmed-author:FabrizioEE,
pubmed-author:FincatiEE,
pubmed-author:GoldwurmSS,
pubmed-author:GuidiMM,
pubmed-author:HorstinkM WMW,
pubmed-author:Italian Parkinson Genetics Network,
pubmed-author:LambertiPP,
pubmed-author:LopianoLL,
pubmed-author:Maat-KievitJ AJA,
pubmed-author:MarconiRR,
pubmed-author:MarkovA AAA,
pubmed-author:MartignoniEE,
pubmed-author:MeczLL,
pubmed-author:MontagnaPP,
pubmed-author:NicholsD SDS,
pubmed-author:OostraB ABA,
pubmed-author:PohlTT,
pubmed-author:SampaioCC,
pubmed-author:StocchiFF,
pubmed-author:TassorelliCC,
pubmed-author:TavellaAA,
pubmed-author:TinazziMM,
pubmed-author:TomsAA,
pubmed-author:VanacoreNN,
pubmed-author:de KleinAA
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pubmed:issnType |
Electronic
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pubmed:day |
12
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pubmed:volume |
65
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
87-95
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:16009891-Adolescent,
pubmed-meshheading:16009891-Adult,
pubmed-meshheading:16009891-Age of Onset,
pubmed-meshheading:16009891-Child,
pubmed-meshheading:16009891-DNA, Complementary,
pubmed-meshheading:16009891-DNA Mutational Analysis,
pubmed-meshheading:16009891-Female,
pubmed-meshheading:16009891-Gene Frequency,
pubmed-meshheading:16009891-Genetic Predisposition to Disease,
pubmed-meshheading:16009891-Genetic Testing,
pubmed-meshheading:16009891-Genome,
pubmed-meshheading:16009891-Genotype,
pubmed-meshheading:16009891-Humans,
pubmed-meshheading:16009891-Italy,
pubmed-meshheading:16009891-Male,
pubmed-meshheading:16009891-Middle Aged,
pubmed-meshheading:16009891-Mutation,
pubmed-meshheading:16009891-Mutation, Missense,
pubmed-meshheading:16009891-Parkinson Disease,
pubmed-meshheading:16009891-Phenotype,
pubmed-meshheading:16009891-Polymorphism, Genetic,
pubmed-meshheading:16009891-Protein Kinases,
pubmed-meshheading:16009891-Sequence Homology, Amino Acid
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pubmed:year |
2005
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pubmed:articleTitle |
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes.
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pubmed:affiliation |
Department of Clinical Genetics, Erasmus MC Rotterdam, The Netherlands. v.bonifati@erasmusmc.nl
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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