Associated Papers
Identification and characterization of novel MPC1 gene variants causing mitochondrial pyruvate carrier deficiency.
Jiang H et al.
Journal of Inherited Metabolic Disease, 2022
34873722 (PubMed )
Supplement: supplement_1.docx
A functional single-nucleotide polymorphism in the human cytidine deaminase gene contributing to ara-C sensitivity.
Yue L et al.
Pharmacogenetics, 2003
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