Two novel cases of compound heterozygous mutations in mitofusin2: Finding out the inheritance

enthalten in: Neuromuscular disorders | 2017

von Geroldi, A. | Lastella, P. | Patruno, M. | +9

Influence of comorbidities on the phenotype of patients affected by Charcot–Marie–Tooth neuropathy type 1A

enthalten in: Neuromuscular disorders | 2013

von Ursino, G. | Alberti, M. | Grandis, M. | +10

A family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci

enthalten in: Neuromuscular disorders | 2002

von Bellone, E. | Rodolico, C. | Toscano, A. | +10