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366 The primary mitochondrial diseases caused by nDNA mutations Given that the majority of mitochondrial proteins are encoded by nDNA, mitochondrial diseases resulting from nDNA mutations encompass not only disturbances in OXPHOS but also defects in various structural or functional proteins essential for mtDNA maintenance, mitochondrial function and structure, and mito-nuclear communication

By activating melanocortin receptors throughout the body, it has also been studied for pathways involved in arousal, appetite regulation, energy balance, inflammatory signaling, and broader neuroendocrine function

Molecular Weight: 173.22 g/mol

Because the study was observational, it cannot prove the medications directly cause hair loss

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