Authors: Eisenberg, I Avidan, N Potikha, T Hochner, H Chen, M Olender, T Barash, M Shemesh, M Sadeh, M Grabov-Nardini, G Shmilevich, I Friedmann, A Karpati, G Bradley, WG Baumbach, L Lancet, D Ben Asher, E Beckmann, JS Argov, Z Mitrani-Rosenbaum, S

Citation: I. Eisenberg et al., The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene ismutated in recessive hereditary inclusion body myopathy, NAT GENET, 29(1), 2001, pp. 83-87