其他Biochemical characterization of the M712T-mutation of the UDP-N-acetylglucosamine 2-epimerase/N-acetyl-mannosaminekinase in hereditary inclusion body myopathy.
期刊:Neuromuscular disorders : NMD发表年份:2011作者:Wenke Weidemann; Anika Reinhardt; Annett Thate; Rüdiger Horstkorte
