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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
19
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pubmed:dateCreated |
2007-5-8
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pubmed:abstractText |
To assess the prevalence, nature, and associated phenotypes of ATP13A2 gene mutations among patients with juvenile parkinsonism (onset <21 years) or young onset (between 21 and 40 years) Parkinson disease (YOPD).
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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 |
May
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pubmed:issn |
1526-632X
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pubmed:author |
pubmed-author:AbbruzzeseGG,
pubmed-author:BarbosaE RER,
pubmed-author:BonifatiVV,
pubmed-author:ChienH FHF,
pubmed-author:Di FonzoAA,
pubmed-author:FabbriniGG,
pubmed-author:FerreiraJ JJJ,
pubmed-author:FincatiEE,
pubmed-author:GiraudoSS,
pubmed-author:GoldwurmSS,
pubmed-author:HorstinkM WMW,
pubmed-author:IlicetoGG,
pubmed-author:Italian Parkinson Genetics Network,
pubmed-author:JardimL BLB,
pubmed-author:LiberaA DallaAD,
pubmed-author:LopianoLL,
pubmed-author:MarconiRR,
pubmed-author:MarkovA AAA,
pubmed-author:MartignoniEE,
pubmed-author:MeczLL,
pubmed-author:MontagnaPP,
pubmed-author:OostraB ABA,
pubmed-author:SocalMM,
pubmed-author:SquitieriFF,
pubmed-author:StocchiFF,
pubmed-author:TassorelliCC
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pubmed:issnType |
Electronic
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pubmed:day |
8
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pubmed:volume |
68
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1557-62
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:17485642-Adolescent,
pubmed-meshheading:17485642-Adult,
pubmed-meshheading:17485642-Age of Onset,
pubmed-meshheading:17485642-Brain,
pubmed-meshheading:17485642-Brazil,
pubmed-meshheading:17485642-Child,
pubmed-meshheading:17485642-Cohort Studies,
pubmed-meshheading:17485642-DNA Mutational Analysis,
pubmed-meshheading:17485642-Diagnosis, Differential,
pubmed-meshheading:17485642-Female,
pubmed-meshheading:17485642-Genetic Predisposition to Disease,
pubmed-meshheading:17485642-Genetic Testing,
pubmed-meshheading:17485642-Genotype,
pubmed-meshheading:17485642-Humans,
pubmed-meshheading:17485642-Italy,
pubmed-meshheading:17485642-Male,
pubmed-meshheading:17485642-Middle Aged,
pubmed-meshheading:17485642-Mutation, Missense,
pubmed-meshheading:17485642-Parkinson Disease,
pubmed-meshheading:17485642-Parkinsonian Disorders,
pubmed-meshheading:17485642-Phenotype,
pubmed-meshheading:17485642-Prevalence,
pubmed-meshheading:17485642-Proton-Translocating ATPases
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pubmed:year |
2007
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pubmed:articleTitle |
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease.
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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,
Case Reports,
Research Support, Non-U.S. Gov't
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