Lingchao Meng
3PUBLICATIONS
2CO-AUTHORS
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Publications (3)
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|Nov 29, 2019
Homozygous splice-site mutation c.78 + 5G>A in PMP22 causes congenital hypomyelinating neuropathy.Rui Wu, Jun Fu, Lingchao Meng
|Aug 22, 2019
A novel mutation in PRPS1 causes X-linked Charcot-Marie-Tooth disease-5.Lingchao Meng, Kang Wang, He Lv
|Apr 09, 2019
Sural nerve pathology in TFG-associated motor neuron disease with sensory neuropathy.Jia Li, Lingchao Meng, Rui Wu
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