Article
GNE myopathy in a Chinese male with a novel homozygous mutation.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia - 1 May 2017
Rui Ban, Chuanqiang Pu, Huifang Wang, Huaxu Liu, Qiang Shi, Miaomiao Wei, Haiwen Song
Abstract excerpt
GNE myopathy is a rare autosomal recessive inheritance disease due to the mutation of GNE gene. To date, 107 mutations have been reported in different populations worldwide in GNE gene(HGMD Professional 2016.2). Here we report a patient of novel homozygous GNE gene mutation from China.
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