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USD 39.95 Prices may be subject to local taxes which are calculated during checkout References Bckhed, F., Manchester, J.K., Semenkovich, C.F

doi: 10.1371/journal.pone.0127271

Primary plasmalemmal carnitine transporter defect manifested with dicarboxylic aciduria and impaired fatty acid oxidation

The DiGeorge syndrome , also called velocardiofacial or 22q11.2 deletion syndrome (22q11.2DS), is caused by a hemizygous microdeletion (1.53 Mb) on chromosome 22 DiGeorge syndrome The prevalence rate of this condition is ~1 in 4000 [356]

Mol Cell Biol 38: e0065417 Blighe K, Rana S, Lewis M (2022) EnhancedVolcano: Publication-ready volcano plots with enhanced colouring and labeling
