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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 |
2005-1-11
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pubmed:abstractText |
Alcohol dehydrogenases (ADHs) may be involved in the pathogenesis of neurodegenerative disorders because of their multiple roles in detoxification pathways and retinoic acid synthesis. In a previous study, significant association of an ADH class IV allele with Parkinson disease (PD) was found in a Swedish sample.
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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:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0003-9942
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pubmed:author |
pubmed-author:AhlbergJarlJ,
pubmed-author:AnvretMariaM,
pubmed-author:AshizawaTetsuoT,
pubmed-author:BuervenichSilviaS,
pubmed-author:CarmineAndreaA,
pubmed-author:EerolaJohannaJ,
pubmed-author:GalterDagmarD,
pubmed-author:GasserThomasT,
pubmed-author:HansonMelissaM,
pubmed-author:HellströmOlliO,
pubmed-author:HolmbergBjörnB,
pubmed-author:JohnelsBoB,
pubmed-author:KlockgetherThomasT,
pubmed-author:MatsuuraTohruT,
pubmed-author:McMahonFrancis JFJ,
pubmed-author:NissbrandtHansH,
pubmed-author:OlsonLarsL,
pubmed-author:ShahabiHaydeh NHN,
pubmed-author:SingletonAndrewA,
pubmed-author:SydowOlofO,
pubmed-author:TienariPentti JPJ,
pubmed-author:WüllnerUllrichU,
pubmed-author:WaseemShamailaS,
pubmed-author:ZimprichAlexanderA
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pubmed:issnType |
Print
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pubmed:volume |
62
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
74-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:15642852-Adult,
pubmed-meshheading:15642852-Aged,
pubmed-meshheading:15642852-Alcohol Dehydrogenase,
pubmed-meshheading:15642852-Alleles,
pubmed-meshheading:15642852-Case-Control Studies,
pubmed-meshheading:15642852-Chi-Square Distribution,
pubmed-meshheading:15642852-Chromosomes, Human, Pair 4,
pubmed-meshheading:15642852-Codon, Terminator,
pubmed-meshheading:15642852-DNA Mutational Analysis,
pubmed-meshheading:15642852-European Continental Ancestry Group,
pubmed-meshheading:15642852-Exons,
pubmed-meshheading:15642852-Female,
pubmed-meshheading:15642852-Humans,
pubmed-meshheading:15642852-Male,
pubmed-meshheading:15642852-Middle Aged,
pubmed-meshheading:15642852-Mutation,
pubmed-meshheading:15642852-Parkinson Disease,
pubmed-meshheading:15642852-Polymorphism, Single Nucleotide
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pubmed:year |
2005
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pubmed:articleTitle |
A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample.
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pubmed:affiliation |
Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden. buervens@intra.nimh.nih.gov
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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