Author:
Di Fonzo Alessio,Jinnah H.A.,Zech Michael
Reference170 articles.
1. Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanisms;Abela;Journal of Inherited Metabolic Disease,2018
2. Phenomenology and classification of dystonia: A consensus update;Albanese;Movement Disorders: Official Journal of the Movement Disorder Society,2013
3. Biallelic mutations in DNAJC12 cause hyperphenylalaninemia, dystonia, and intellectual disability;Anikster;American Journal of Human Genetics,2017
4. HPCA confirmed as a genetic cause of DYT2-like dystonia phenotype;Atasu;Movement Disorders: Official Journal of the Movement Disorder Society,2018
5. The effect of sodium channels on neurological/neuronal disorders: A systematic review;Bagheri;International Journal of Developmental Neuroscience: The Official Journal of the International Society for Developmental Neuroscience,2021
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