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Spinal and bulbar muscular atrophy and Charcot–Marie–Tooth type 1A: Co-existence of two rare neuromuscular genetic diseases in the same patient
Sagnelli, Anna, Scaioli, Vidmer, Piscosquito, Giuseppe, Salsano, Ettore, Dalla Bella, Eleonora, Gellera, Cinzia, Pareyson, DavideVolume:
25
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2015.07.015
Date:
October, 2015
File:
PDF, 363 KB
english, 2015