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An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptorMONNIER, Nicole; ROMERO, Norma Beatriz; LERALE, Joëlle et al.Human molecular genetics (Print). 2000, Vol 9, Num 18, pp 2599-2608, issn 0964-6906Article

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Muscle histone deacetylase 4 upregulation in amyotrophic lateral sclerosis: potential role in reinnervation ability and disease progressionBRUNETEAU, Gaëlle; SIMONET, Thomas; HELL-REMY, Caroline et al.Brain. 2013, Vol 136, pp 2359-2368, issn 0006-8950, 10 p., 8Article