Varaico: Literature-Extracted Genetic Variants

Gene:LRRK2
Variant:p.E1724Splc
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LRRK2

NM_198578.4:p.E1724Splc

Associated Papers

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

Janković MZ et al.

Journal of the Neurological Sciences, 2015

Analysis of Leucine-rich repeat kinase 2 (LRRK2) and Parkinson protein 2 (parkin, PARK2) genes mutations in Slovak Parkinson disease patients.

Bognar C et al.

General Physiology and Biophysics, 2013

Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe.

Rubio JP et al.

Human Mutation, 2012

Evaluation of the role of LRRK2 gene in Parkinson's disease in an East Indian cohort.

Sadhukhan T et al.

Disease Markers, 2012

The LRRK2 Arg1628Pro variant is a risk factor for Parkinson's disease in the Chinese population.

Lu CS et al.

Neurogenetics, 2008

LRRK2 screening in a Canadian Parkinson's disease cohort.

Grimes DA et al.

The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques, 2007

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."