Clinical and genetic characteristcs of hereditary motor and sensory neuropathy type IIA
In this study, clinical manifestations of hereditary motor andsensory neuropathy type IIA (HMSN IIA, orCharcotMarieTooth disease type 2A) were analyzed in 22patients with the disease caused by different mutations of theMFN2 gene. Molecular genetic analysis showed that in theexamined cohort of Russia...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Research Center of Neurology
2017-02-01
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Series: | Анналы клинической и экспериментальной неврологии |
Subjects: | |
Online Access: | https://annaly-nevrologii.com/journal/pathID/article/viewFile/422/320 |