cacna1

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    Periodic Paralysis Across the Life Course: Age-related Phenotype transition and sarcopenia overlap, 2024, Suetterlin et al

    Interesting study that explores RYR1 gene variations and their import to things like muscle weakness and ATP and mitochondrial function, and how these change with age in healthy individuals vs those with channelopathies. RYR1 variations have been tied into ME/CFS before. This study parses down...
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