Publications by authors named "Bernard Bricka"

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SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations.
Stéphanie Millecamps, François Salachas, Cécile Cazeneuve, Paul Gordon, Bernard Bricka

J Med Genet· August 2010

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A de novo SPAST mutation leading to somatic mosaicism is associated with a later age at onset in HSP.
Christel Depienne, Estelle Fedirko, Jean-Marc Faucheux, Sylvie Forlani, Bernard Bricka

Neurogenetics· August 2007

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