Publication: Sorbitol-dehydrogenase (SORD) gene mutation as a curable cause of charcot-marie-tooth 2 (CMT-2) and distal hereditary motor neuronopathy (D-HMN)
Program
KU Authors
Co-Authors
Advisor
Publication Date
2022
Language
English
Type
Meeting Abstract
Journal Title
Journal ISSN
Volume Title
Abstract
N/A
Description
Source:
Journal of the Peripheral Nervous System
Publisher:
Wiley
Keywords:
Subject
Clinical neuropsychology, Neurosciences