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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

Author:

Anna Sagnelli,Vidmer Scaioli,Giuseppe Piscosquito,Ettore Salsano,Eleonora Dalla Bella,Cinzia Gellera,Davide Pareyson

Publication:

Neuromuscular Disorders

Publisher:

Elsevier

Date:

October 2015

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