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PDFOriginal article
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations
- 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
Citation
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
July 23, 2010
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- Previous version (24 June 2010).
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© 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.