Editorial: Genetic advances and translational applications in movement disorders
Author:
Publisher
Frontiers Media SA
Subject
Neurology (clinical),Neurology
Reference6 articles.
1. Challenges in clinicogenetic correlations: one phenotype – many genes;Gannamani;Mov Disord Clin Pract.,2021
2. Challenges in clinicogenetic correlations: one gene - many phenotypes;Magrinelli;Mov Disord Clin Pract.,2021
3. Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia;Cortese;Nat Genet.,2019
4. Standards of NGS data sharing and analysis in ataxias: recommendations by the NGS working group of the ataxia global initiative;Beijer;Cerebellum.,2023
5. What we don't need to prove but need to do in multidisciplinary treatment and care in Huntington's disease: a position paper;Mühlbäck;Orphanet J Rare Dis.,2023
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