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rdf:type |
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lifeskim:mentions |
umls-concept:C0017382,
umls-concept:C0026882,
umls-concept:C0030567,
umls-concept:C0035647,
umls-concept:C0205309,
umls-concept:C0376249,
umls-concept:C1513822,
umls-concept:C1833334,
umls-concept:C1843571,
umls-concept:C1850419,
umls-concept:C1880171,
umls-concept:C1970036,
umls-concept:C2603343
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pubmed:issue |
9
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pubmed:dateCreated |
2010-9-14
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pubmed:abstractText |
To assess the frequency and clinical characteristics of carriers of previously identified mutations in 6 genes associated with early-onset Parkinson disease (PD) and provide empirical data that can be used to inform genetic counseling.
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pubmed:grant |
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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:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1538-3687
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pubmed:author |
pubmed-author:AlcalayRoy NRN,
pubmed-author:AndrewsHowardH,
pubmed-author:BressmanSusan BSB,
pubmed-author:CaccappoloEliseE,
pubmed-author:ClarkLorraine NLN,
pubmed-author:ColcherAmyA,
pubmed-author:ComellaCynthiaC,
pubmed-author:CoteLucienL,
pubmed-author:FahnStanleyS,
pubmed-author:FordBlairB,
pubmed-author:FriedmanJoseph HJH,
pubmed-author:FruchtStevenS,
pubmed-author:HinerBradleyB,
pubmed-author:JenningsDannaD,
pubmed-author:KisselevSergeyS,
pubmed-author:LouisElan DED,
pubmed-author:MarderKarenK,
pubmed-author:MarshLauraL,
pubmed-author:Mejia-SantanaHelenH,
pubmed-author:MickelSusanS,
pubmed-author:NanceMartha AMA,
pubmed-author:NovakKevinK,
pubmed-author:OttmanRuthR,
pubmed-author:PfeifferRonaldR,
pubmed-author:RezakMichaelM,
pubmed-author:RosadoLlencyL,
pubmed-author:RossBarbara MBM,
pubmed-author:ScottWilliam KWK,
pubmed-author:SiderowfAndrewA,
pubmed-author:TangMing XinMX,
pubmed-author:TannerCarolineC,
pubmed-author:VerbitskyMiguelM,
pubmed-author:WatersCherylC
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pubmed:issnType |
Electronic
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pubmed:volume |
67
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1116-22
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pubmed:meshHeading |
pubmed-meshheading:20837857-Adult,
pubmed-meshheading:20837857-Age Factors,
pubmed-meshheading:20837857-Age of Onset,
pubmed-meshheading:20837857-Cross-Sectional Studies,
pubmed-meshheading:20837857-Female,
pubmed-meshheading:20837857-Gene Frequency,
pubmed-meshheading:20837857-Genetic Counseling,
pubmed-meshheading:20837857-Genetic Predisposition to Disease,
pubmed-meshheading:20837857-Genetic Testing,
pubmed-meshheading:20837857-Genotype,
pubmed-meshheading:20837857-Hispanic Americans,
pubmed-meshheading:20837857-Humans,
pubmed-meshheading:20837857-Jews,
pubmed-meshheading:20837857-Male,
pubmed-meshheading:20837857-Middle Aged,
pubmed-meshheading:20837857-Mutation,
pubmed-meshheading:20837857-Parkinson Disease,
pubmed-meshheading:20837857-Regression Analysis,
pubmed-meshheading:20837857-Risk,
pubmed-meshheading:20837857-United States
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pubmed:year |
2010
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pubmed:articleTitle |
Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease study.
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pubmed:affiliation |
Department of Neurology, Columbia University, New York, NY 10032, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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