|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
11
|
|
pubmed:dateCreated |
2005-11-7
|
|
pubmed:abstractText |
Mutations in the gene Leucine-Rich Repeat Kinase 2 (LRRK2) were recently identified as the cause of PARK8 linked autosomal dominant Parkinson's disease.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Nov
|
|
pubmed:issn |
1468-6244
|
|
pubmed:author |
pubmed-author:AntoniniAA,
pubmed-author:BarbosaEE,
pubmed-author:Bertoli-AvellaA MAM,
pubmed-author:BonifatiVV,
pubmed-author:BreedveldG JGJ,
pubmed-author:CaneseAA,
pubmed-author:ChienH FHF,
pubmed-author:Dalla LiberaAA,
pubmed-author:Di FonzoAA,
pubmed-author:DiromaCC,
pubmed-author:FabrizioEE,
pubmed-author:FerreiraJJ,
pubmed-author:GoldwurmSS,
pubmed-author:LambertiPP,
pubmed-author:MarianiCC,
pubmed-author:MeczLL,
pubmed-author:MeucciNN,
pubmed-author:OostraB ABA,
pubmed-author:PezzoliGG,
pubmed-author:PohlTT,
pubmed-author:SacilottoGG,
pubmed-author:SalaniGG,
pubmed-author:SampaioCC,
pubmed-author:SimonsE JEJ,
pubmed-author:SironiFF,
pubmed-author:StocchiFF,
pubmed-author:TeseiSS,
pubmed-author:VanacoreNN,
pubmed-author:ZecchinelliAA,
pubmed-author:ZiniMM
|
|
pubmed:issnType |
Electronic
|
|
pubmed:volume |
42
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
e65
|
|
pubmed:dateRevised |
2008-11-20
|
|
pubmed:meshHeading |
pubmed-meshheading:16272257-Adult,
pubmed-meshheading:16272257-Aged,
pubmed-meshheading:16272257-Alleles,
pubmed-meshheading:16272257-Base Sequence,
pubmed-meshheading:16272257-Female,
pubmed-meshheading:16272257-Founder Effect,
pubmed-meshheading:16272257-Heterozygote,
pubmed-meshheading:16272257-Humans,
pubmed-meshheading:16272257-Male,
pubmed-meshheading:16272257-Middle Aged,
pubmed-meshheading:16272257-Molecular Sequence Data,
pubmed-meshheading:16272257-Mutation,
pubmed-meshheading:16272257-Parkinson Disease,
pubmed-meshheading:16272257-Protein-Serine-Threonine Kinases
|
|
pubmed:year |
2005
|
|
pubmed:articleTitle |
The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor.
|
|
pubmed:affiliation |
Parkinson Institute, Istituti Clinici di Perfezionamento, Milan, Italy.
|
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
