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Updated: Sep 10, 2025

Functional Characterization of Endogenously Expressed Human RYR1 Variants
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Functional Characterization of Endogenously Expressed Human RYR1 Variants

Published on: June 9, 2021

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与RYR1相关的神经病变中的NAD+失恒

Tokunbor A Lawal1,2, Willa Riekhof1, Linda Groom3

  • 1Skeletal Myopathies Unit, Translational Biobehavioral and Health Disparities Branch, NIH Clinical Center, National Institutes of Health, Bethesda, MD, USA.

Skeletal muscle
|August 22, 2025
PubMed
概括

在RYR1相关的肌肉病患者中,NAD+缺乏是常见的. 补充尼古丁胺核酸 (NR) 显示有可能改善患者衍生细胞的细胞能量产生.

关键词:
时间:遗传性肌肉病葡萄糖其他类型其他国家氧化应激

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