Rui Wu
3PUBLICATIONS
3CO-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
|Jul 17, 2018
Late-onset hereditary sensory and autonomic neuropathy expands the phenotypic spectrum of MFN2-related diseases.Rui Wu, Jun Fu, Lingchao Meng
|Aug 25, 2017
Clinical and Pathological Variation of Charcot-Marie-Tooth 1A in a Large Chinese Cohort.Rui Wu, He Lv, Wei Zhang
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