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