Prevalence of the H1069Q mutation in ATP7B in discordant pairs with early-onset Parkinson's Disease

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Bibliographic Details
Published in:Movement disorders 2006-10, Vol.21 (10), p.1789-1790
Main Authors: Möller, Jens Carsten, Leinweber, Barbara, Rissling, Ida, Oertel, Wolfgang Herman, Bandmann, Oliver, Schmidt, Hartmut H.-J.
Format: Article
Language:English
Subjects:
Adenosine Triphosphatases - genetics
Adult
Age Factors
Aged
Alleles
Cation Transport Proteins - genetics
Copper-transporting ATPases
Exons - genetics
Female
Genotype
Hepatolenticular Degeneration - diagnosis
Hepatolenticular Degeneration - genetics
Humans
Male
Middle Aged
Mutation - genetics
Parkinson Disease - diagnosis
Parkinson Disease - genetics
Phenotype
Siblings
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ISSN:0885-3185
1531-8257
DOI:10.1002/mds.21066