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