Two inherited diseases in the carnitine biosynthetic pathway have been reported (deficiency of 6- N -trimethyllysine dioxygenase and deficiency of -butyrobetaine dioxygenase), which result in only mildly decreased to normal carnitine levels in the affected patients [60, 61]
As our understanding of these "miracle" peptides grows, they are becoming a versatile tool for improving the overall quality of life
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