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Original article
Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity
  1. Correspondence to Dr Sabrina Sacconi, Centre de référence des maladies neuromusculaires, Archet 1 Hospital, 151 Route de Saint Antoine de Ginestière, 06000 Nice, France; sacconi{at}unice.fr
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Citation

Sacconi S, Camaño P, de Greef JC, et al
Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity

Publication history

  • Received April 4, 2011
  • Revised August 29, 2011
  • Accepted August 30, 2011
  • First published October 7, 2011.
Online issue publication 
December 13, 2011

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