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Cardiolipin deficiency leads to the destabilization of mitochondrial magnesium channel MRS2 in Barth syndrome.
- Published in:
- Human Molecular Genetics, 2023, v. 32, n. 24, p. 3353, doi. 10.1093/hmg/ddad153
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- Publication type:
- Article
MCU-complex-mediated mitochondrial calcium signaling is impaired in Barth syndrome.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 3, p. 376, doi. 10.1093/hmg/ddab254
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- Publication type:
- Article