Congenital Disorder of Glycosylation Type 1T with a Novel...

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Neuromuscular Disorders 2019 / 1

Congenital Disorder of Glycosylation Type 1T with a Novel Truncated Homozygous Mutation in PGM1 Gene and Literature Review

Tian, Wo-Tu, Luan, Xing-Hua, Zhou, Hai-Yan, Zhang, Chao, Huang, Xiao-Jun, Liu, Xiao-Li, Chen, Sheng-Di, Tang, Hui-Dong, Cao, Li
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Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2019.01.001
Date:
January, 2019
File:
PDF, 1.16 MB
english, 2019
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