Identification of a Novel <i>de Novo</i> Variant in the <i>SYT2</i> Gene Causing a Rare Type of Distal Hereditary Motor Neuropathy
Objective: To report the first <i>de novo</i> missense mutation in the <i>SYT2</i> gene causing distal hereditary motor neuropathy. Methods: Genetic testing was carried out, including clinical exome sequencing for the proband and Sanger sequencing for the proband and his pare...
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2020-10-01
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Series: | Genes |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4425/11/11/1238 |