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Results: 3

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: Bargal, R Avidan, N Olender, T Ben Asher, E Zeigler, M Raas-Rothschild, A Frumkin, A Ben-Yoseph, O Friedlender, Y Lancet, D Bach, G
Citation: R. Bargal et al., Mucolipidosis type IV: Novel MCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish population, HUM MUTAT, 17(5), 2001, pp. 397-402

Authors: Lahat, H Pras, E Olender, T Avidan, N Ben-Asher, E Man, O Levy-Nissenbaum, E Khoury, A Lorber, A Goldman, B Lancet, D Eldar, M
Citation: H. Lahat et al., A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel, AM J HU GEN, 69(6), 2001, pp. 1378-1384
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