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Article

[The absence of the common LRRK2 G2019S mutation in 120 young onset Hungarian Parkinon's disease patients].

Ideggyogyaszati szemle - 30 Jul 2012

Balicza Péter, Bereznai Benjamin, Takáts Annamária, Klivényi Péter, Dibó György, Hidasi Eszter, Balogh István, Molnár Mária Judit

Abstract excerpt

Parkinson's disease is a promising target of applying personalized medicine. For this purpose it is crucial to reveal the genetic and environmental factors, which contribute to the disease, also to collect epidemiologic data and to preserve the patients samples and data in a proper biobank. In our investigation we examined the prevalence of the most frequent Parkinson's disease causing LRRK2 G2019S mutation in a...

Topics

Adult
Age of Onset
Aged
Female
Gene Frequency
Genetic Predisposition to Disease
Genetic Testing
Glycine
Humans
Hungary
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Male

Middle Aged

Parkinson Disease

Point Mutation

Protein Serine-Threonine Kinases

Serine

Source

Identifiers

PMID: 23074843

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026.

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