Autosomal Recessive Mitochondrial Myopathy due to MICU-1 Variants
Author:
Affiliation:
1. Department of Neurological, Neurology and Neurophysiology Center, Vienna, Austria
Publisher
Medknow
Subject
Neurology (clinical)
Reference6 articles.
1. Mitochondrial calcium uptake 1 (MICU1) gene-related myopathy with extrapyramidal signs:A clinico-radiological case report from India;Mukherjee;Ann Indian Acad Neurol,2023
2. MICU1 regulates mitochondrial cristae structure and function independently of the mitochondrial Ca2+ uniporter channel;Tomar;Sci Signal,2023
3. Reporting a rare form of myopathy, myopathy with extrapyramidal signs, in an Iranian family using next generation sequencing:A case report;Mojbafan;BMC Med Genet,2020
4. Molecular pathophysiology of human MICU1 deficiency;Kohlschmidt;Neuropathol Appl Neurobiol,2021
5. Melatonin alleviates angiotensin-II-induced cardiac hypertrophy via activating MICU1 pathway;Yang;Aging (Albany NY),2020
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