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[95] In addition to this, mutations in genes related to lysine metabolism have been implicated in several disease states, including pyridoxine-dependent epilepsia (ALDH7A1 gene), -ketoadipic and -aminoadipic aciduria (DHTKD1 gene), and glutaric aciduria type 1 (GCDH gene)
The molecule itself, without the vesicle architecture, for those approaching the category in its most direct form
Chan, D
Frontiers in endocrinology, 3, 131
Sources Pickart L, Margolina A (2018)
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