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Article

Identification of novel variants in LRRK2 gene in patients with Parkinson's disease in Serbian population.

Journal of the neurological sciences - 1 Jan 2015

Janković Milena Z, Kresojević Nikola D, Dobričić Valerija S, Marković Vladana V, Petrović Igor N, Novaković Ivana V, Kostić Vladimir S

Abstract excerpt

BACKGROUND: Mutations in LRRK2 (leucine-rich repeat kinase 2) are the most common cause of autosomal dominant Parkinson's disease (PD). Large international studies have revealed that pathogenic mutations are clustered in several exons coding for functional domains of LRRK2 protein, but the mutation frequency differs among populations. Systematic study of LRRK2 mutation prevalence and phenotype in Serbian...

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Identifiers

PMID: 25899316
DOI: 10.1016/j.jns.2015.04.002

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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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