From Genotype to Phenotype: Investigating SLC22A5 Variants and Their Significance in Carnitine Deficiency: A Systematic Review Study.

J Cell Mol Med · 2026 · PMC13387816 · PMID 42480505

Europe PMC DOI

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a possible trendno p-value reported

Therefore, although these findings may indicate a possible trend, they should be interpreted with caution.

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