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Metrika 55 , 125138 (2002)
Genetic CPT1A deficiency is a very rare occurrence, but patients generally present with hypoketotic hypoglycemia and hepatic encephalopathy due to defects in long-chain FAO (27)
10.1016/j.atherosclerosis.2013.10.029 Atherosclerosis 98 RousselJ.ThireauJ.BrennerC.SaintN.ScheuermannV.LacampagneA.et al (2015)
Treatment of Central Disorders of Hypersomnolence: an American Academy of Sleep Medicine Clinical Practice Guideline. Journal of Clinical Sleep Medicine, 2021, doi:10.5664/jcsm.9328
