Frontiers Newborn Screening and Genetic Analysis Identify Six Novel Genetic Variants for Primary Carnitine Deficiency in Ningbo Area, China Carnitine metabolism and fatigue. Medical conditions that may present Download Table Carnitine Acylcarnitine Translocase Deficiency Disorder DoveMed Reversible weakness and encephalopathy while on long term valproate treatment due to carnitine deficiency BMJ Case Reports Carnitine is necessary to maintain the phenotype and function of brown adipose tissue Laboratory Investigation Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2020;25:23 29]
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