Two Novel De Novo GARS Mutations Cause Early-Onset Axonal Charcot-Marie-Tooth Disease
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference30 articles.
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1. Dominant aminoacyl-tRNA synthetase disorders: lessons learned from in vivo disease models;Frontiers in Neuroscience;2023-05-12
2. Pathogenic missense variants altering codon 336 of GARS1 lead to divergent dominant phenotypes;Human Mutation;2022-04-21
3. Infantile‐onset CMT2D/dSMA‐V in a Chinese family with parental germline mosaicism for a novel mutation in the GARS1 gene;Molecular Genetics & Genomic Medicine;2021-12-12
4. Variants of aminoacyl‐tRNA synthetase genes in Charcot‐Marie‐Tooth disease: A Korean cohort study;Journal of the Peripheral Nervous System;2021-12
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