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SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations
  1. Correspondence to Dr Stéphanie Millecamps, Hôpital Pitié-Salpêtrière, CRICM UMR_S975, Bât Pharmacie - 4ème étage, 47 bd de l'Hôpital, 75651 Paris cedex 13, France; stephanie.millecamps{at}upmc.fr
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Millecamps S, Salachas F, Cazeneuve C, et al
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations

Publication history

  • Received January 14, 2010
  • Revised March 11, 2010
  • Accepted March 15, 2010
  • First published June 24, 2010.
Online issue publication 
April 27, 2016

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