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A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease

scientific article published in The Lancet

Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease

artículo científico publicado en 2006

GIGYF2 mutations are not a frequent cause of familial Parkinson's disease

artículo científico publicado en 2009

LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study

scholarly article by Marialuisa Quadri et al published July 2018 in Lancet Neurology

Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family

scientific article published on 31 July 2019

Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent dataset

artículo científico publicado en 2002

Muscle ceroid lipofuscin-like deposits in a patient with corticobasal syndrome due to a progranulin mutation

scientific article published on 22 May 2017

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

artículo científico publicado en 2003

The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN.

artículo científico publicado en 2017

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