The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
Iris Eisenberg(Hadassah Medical Center), Nili Avidan(Weizmann Institute of Science), Tamara Potikha(Hadassah Medical Center), Hagit Hochner(Hadassah Medical Center), Miriam Chen(Weizmann Institute of Science), Tsviya Olender(Weizmann Institute of Science), Mark Barash(Hadassah Medical Center), Moshe Shemesh(Hadassah Medical Center), Menachem Sadeh(Wolfson Medical Center), Gil Grabov-Nardini(Hadassah Medical Center), Inna Shmilevich(Hadassah Medical Center), A. Friedmann(Hadassah Medical Center), George Karpati(Montreal Neurological Institute and Hospital), Walter G. Bradley(University of Miami), Lisa Baumbach(University of Miami), Doron Lancet(Weizmann Institute of Science), Edna Ben Asher(Weizmann Institute of Science), J. Beckmann(Weizmann Institute of Science), Zohar Argov(Hadassah Medical Center), Stella Mitrani‐Rosenbaum(Hadassah Medical Center)
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