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Identity should be confirmed by mass spectrometry matching the expected 5135.9 Da molecular weight
doi: 10.3390/ijms222011128 34 de la RocheMHamiltonCMortensenRJeyaprakashAAGhoshSAnandPK
21 Heriditary cystatin C amyloid angiopathy (HCCAA): Hereditary cystatin C amyloid angiopathy (HCCAA) is a rare dominantly inherited disease caused by a leucine to glutamine variant of human cystatin C (hCC)
Medical supervision also matters because history is not always obvious from a checkbox
reported that in MITOL knockdown-mediated ferroptosis in cardiomyocytes, knockdown of ChaC1 reversed cell injury and increased GSH [53]
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