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BMC Geriatr 21(1):415 2021 PMC8258273 Kanter JE

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Metabolic myopathies with an identified genetic mutation that has subsequently been found in patients presenting with SRM include: adenosine monophosphate deaminase ( AMPD1 ) deficiency (formerly myoadenylate deaminase deficiency) [129], carnitine palmitoyltransferase 2 ( CPT2 ) deficiency [129], glycogen storage diseases II (Pompe disease

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High expression of a novel carnitine palmitoyltransferase-I like protein in rat brown adipose-tissue and heartisolation and characterization of its Cdna clone