Myotonic Dystrophy-1 and Parkinson’s Disease: Clarify the Role of CTG-repeat Size and Variants in VPS13C, SYNJ1, and DNAJC6
Author:
Affiliation:
1. Neurology and Neurophysiology Center, Vienna, Austria
2. Disciplina de Neurociência, Universidade Federal de São Paulo/Escola Paulista de Medicina (UNIFESP/EPM), São Paulo, Brazil
Publisher
Medknow
Subject
Neurology (clinical)
Reference6 articles.
1. Myotonic dystrophy type 1-An atypical presentation having symmetric Parkinsonism and early proximal muscle involvement;Misra;Ann Indian Acad Neurol,2023
2. Recessive mutations in VPS13D cause childhood onset movement disorders;Gauthier;Ann Neurol,2018
3. Parkinson’s disease risk genes act in glia to control neuronal α-synuclein toxicity;Olsen;Neurobiol Dis,2021
4. SYNJ1 gene associated with neonatal onset of neurodegenerative disorder and intractable seizure;Al Zaabi;Mol Genet Genomic Med,2018
5. Clinical variability of SYNJ1-associated early-onset Parkinsonism;Lesage;Front Neurol,2021
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