Wide phenotypic spectrum in axonal Charcot–Marie–Tooth neuropathy type 2 patients with KIF5A mutations
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Title
Wide phenotypic spectrum in axonal Charcot–Marie–Tooth neuropathy type 2 patients with KIF5A mutations
Authors
Keywords
Axonal neuropathy, CMT2, Exome, Hereditary spastic paraplegia (HSP), <em class=EmphasisTypeItalic >KIF5A</em>, Korean
Journal
Genes & Genomics
Volume 40, Issue 1, Pages 77-84
Publisher
Springer Nature
Online
2017-10-10
DOI
10.1007/s13258-017-0612-x
References
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