l-carnitine deficiency snp Frontiers A common X-linked inborn error
A common X linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism PNAS Carnitine deficiency and liver cirrhosis. Download Scientific Diagram The Role of L Carnitine in Kidney Disease and Related Metabolic Dysfunctions Carnitine: Genetic Variants Affecting Mitochondrial Energy and Health Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2020;25:23 29] Phenotype and genotype variation in primary carnitine deficiency Genetics in Medicine
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