Az LRRK2 gyakori G2019S-mutációjának hiánya 120, korai kezdetu magyar Parkinson-beteg esetében

Translated title of the contribution: The absence of the common LRRK2 G2019S mutation in 120 young onset Hungarian Parkinon's disease patients

Péter Balicza, B. Bereznai, Annamária Takáts, P. Klivényi, G. Dibó, Eszter Hidasi, I. Balogh, Mária Judit Molnár

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

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 Hungarian Parkinson-patient group. From 120 patients, we haven't detected this substitution in anyone. Our investigation suggest that the mutation LRRK2 G2019S may be a rare cause of Parkinson disease in the Hungarian population.

Original languageHungarian
Pages (from-to)239-242
Number of pages4
JournalIdeggyógyászati szemle
Volume65
Issue number7-8
Publication statusPublished - Jul 30 2012

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Parkinson Disease
Mutation
Precision Medicine
Population

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

Cite this

Az LRRK2 gyakori G2019S-mutációjának hiánya 120, korai kezdetu magyar Parkinson-beteg esetében. / Balicza, Péter; Bereznai, B.; Takáts, Annamária; Klivényi, P.; Dibó, G.; Hidasi, Eszter; Balogh, I.; Molnár, Mária Judit.

In: Ideggyógyászati szemle, Vol. 65, No. 7-8, 30.07.2012, p. 239-242.

Research output: Contribution to journalArticle

Balicza, Péter ; Bereznai, B. ; Takáts, Annamária ; Klivényi, P. ; Dibó, G. ; Hidasi, Eszter ; Balogh, I. ; Molnár, Mária Judit. / Az LRRK2 gyakori G2019S-mutációjának hiánya 120, korai kezdetu magyar Parkinson-beteg esetében. In: Ideggyógyászati szemle. 2012 ; Vol. 65, No. 7-8. pp. 239-242.
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