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)

Condition:   HIBMInterventions:   Other: motor function and strength assessment;   Other: NMR assessment;   Other: 24h urine and serum collectionSponsor:   Institut de Myologie, FranceRecruiting - verified April 2014
Source: ClinicalTrials.gov - Category: Research Source Type: clinical trials