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, Agnès Camuzat, Léna Guillot-Noël, Odile Russaouen, Gaëlle Bruneteau, Pierre-François Pradat, Nadine Le Forestier, Nadia Vandenberghe, Véronique Danel-Brunaud, Nathalie Guy, Christel Thauvin-Robinet, Lucette Lacomblez, Philippe Couratier, Didier Hannequin, Danielle Seilhean, Isabelle Le Ber, Philippe Corcia, William Camu, Alexis Brice, Guy Rouleau, Eric LeGuern, Vincent Meininger
Journal of Medical Genetics Aug 2010, 47 (8) 554-560; DOI: 10.1136/jmg.2010.077180