lipid metabolism):肉鹼棕櫚醯基轉移酶缺乏症第一型(英语:CarnitinepalmitoyltransferaseI deficiency)和第二型(英语:Carnitinepalmitoyltransferase II deficiency)、醯基輔酶A去氫酶(英语:acyl CoA
Alicia; Vallance, Hilary D.; Waters, Paula J. The paradox of the carnitinepalmitoyltransferase type Ia P479L variant in Canadian Aboriginal populations. Molecular