Clinical, Biological and NMR Outcome Measures Study for Hereditary Inclusion Body Myopathy Due to Mutation of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine Kinase Gene (GNE)

Conditions

• HIBM

Interventions

• OTHER: motor function and strength assessment
• OTHER: NMR assessment
• OTHER: 24h urine and serum collection

Sponsor

Institut de Myologie, France