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