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Re:The mitochondrial NAD+ transporter SLC25A51 is a fasting-... by zamalek on Monday August 08, 2022 @02:01PM (#32388840)
It's a pretty common mutation that severely inhibits (depending on how many of the genes are mutated) methylation of folate in the liver. This is an important source of methyl groups for chemical processes, such as those that include NAD.

There's plenty more on Google, including the interaction between an MTHFR mutation and NAD supplementation.

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