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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

Authors: Eisenberg, I Hochner, H Shemesh, M Levi, T Potikha, T Sadeh, M Argov, Z Jackson, CL Mitrani-Rosenbaum, S
Citation: I. Eisenberg et al., Physical and transcriptional map of the hereditary inclusion body myopathylocus on chromosome 9p12-p13, EUR J HUM G, 9(7), 2001, pp. 501-509
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