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Article

GBA-associated Parkinson's disease in Hungary: clinical features and genetic insights.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology - 1 Jun 2024

Szlepák Tamás, Kossev Annabel P, Csabán Dóra, Illés Anett, Udvari Szabolcs, Balicza Péter, Borsos Beáta, Takáts Annamária, Klivényi Péter, Molnár Mária J

Abstract excerpt

INTRODUCTION: Parkinson's disease (PD) has a complex genetic background involving both rare and common genetic variants. Although a small percentage of cases show a clear Mendelian inheritance pattern, it is much more relevant to identify patients who present with a complex genetic profile of risk variants with different severity. The ß-glucocerebrosidase coding gene (GBA1) is recognized as the most frequent...

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Identifiers

PMID: 38153678
DOI: 10.1007/s10072-023-07213-w
PMCID: PMC11082009

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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