Perturbed Ca2+-dependent signaling of DYT2 hippocalcin mutant as mechanism of autosomal recessive dystonia
Author:
Funder
National Academy of Sciences of Ukraine
Osteopathic Heritage Foundation
Publisher
Elsevier BV
Subject
Neurology
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1. Genetics and Pathogenesis of Dystonia;Annual Review of Pathology: Mechanisms of Disease;2024-01-24
2. Benign Hereditary Chorea as a Manifestation of HPCA Mutation;Movement Disorders Clinical Practice;2022-10-10
3. Childhood‐Onset Choreo‐Dystonia Due to a Recurrent Novel Homozygous Nonsense HPCA Variant: Case Series and Literature Review;Movement Disorders Clinical Practice;2022-08-23
4. Genetic Dystonias: Update on Classification and New Genetic Discoveries;Current Neurology and Neuroscience Reports;2021-02-09
5. Hippocalcin Distribution between the Cytosol and Plasma Membrane of Living Cells;Neurophysiology;2020-01
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