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A novel homozygous splicing mutation of the AGL gene in a Chinese patient with severe myopathy involvement of glycogen storage disease type IIIa.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology - 1 Apr 2021

Li Ying, Qi Xueliang, Zhang Wei, Feng Liqun, Yuan Yun

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PMID: 33175268
DOI: 10.1007/s10072-020-04883-8

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