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10. FSHD / OPMD / MYOTONIC DYSTROPHY

20. Progress in Drug Research / Fortschritte der Arzneimittelforschung / Progrès des recherches pharmaceutiques

21. MYOFIBRILLAR AND DISTAL MYOPATHIES

22. NEW GENES, FUNCTIONS AND BIOMARKERS

24. PRUNE1 ‐related disorder: Expanding the clinical spectrum

25. Confirmation of SLC5A7 ‐related distal hereditary motor neuropathy 7 in a family outside Wales

28. Expression of ecto-nucleoside triphosphate diphosphohydrolases-2 and -3 by the enteric nervous system impacts inflammation in experimental colitis and Crohn’s disease

35. Mutations in DNMT3B Modify Epigenetic Repression of the D4Z4 Repeat and the Penetrance of Facioscapulohumeral Dystrophy

37. Alu-mediated copy number variants in GNE myopathy

40. Gene variants in SMCHD1 and DNMT3B modify the risk for FSHD

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