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American Journal of Human Genetics|March 19, 2002
Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60Jens Jacob Hansen, Alexandra Dürr, Isabelle Cournu-Rebeix, et al.
Annals of Neurology|October 22, 2005
G2019S LRRK2 mutation in French and North African families with Parkinson's diseaseSuzanne Lesage, Pablo Ibanez, Ebba Lohmann, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 9, 2007
A conditional pan-neuronal Drosophila model of spinocerebellar ataxia 7 with a reversible adult phenotype suitable for identifying modifier genesMorwena Latouche, Christelle Lasbleiz, Elodie Martin, et al.
Plos One|March 6, 2014
Heterogeneous pattern of selective pressure for PRRT2 in human populations, but no association with autism spectrum disordersGuillaume Huguet, Caroline Nava, Nathalie Lemière, et al.
JAMA Neurology|June 25, 2014
Charcot-Marie-Tooth disease type 2A: from typical to rare phenotypic and genotypic featuresFrancesco Bombelli, Tanya Stojkovic, Odile Dubourg, et al.
Human Genetics|July 3, 2007
A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3Sylvain Hanein, Alexandra Dürr, Pascale Ribai, et al.
Neurobiology of Disease|December 18, 2003
The C289G and C418R missense mutations cause rapid sequestration of human Parkin into insoluble aggregatesWen-Jie Gu, Olga Corti, Francisco Araujo, et al.
Neurobiology of Aging|December 17, 2009
Follow-up study of the GIGYF2 gene in French families with Parkinson's diseaseSuzanne Lesage, Christel Condroyer, Ebba Lohman, et al.
Acta Neurologica Scandinavica|July 11, 2018
LRRK2 G2019S Parkinson's disease with more benign phenotype than idiopathicSawssan Ben Romdhan, Nouha Farhat, Amina Nasri, et al.
European Journal of Human Genetics : EJHG|December 19, 2008
Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patientsDelia Lorenz, Stephan Klebe, Giovanni Stevanin, et al.
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