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Mutations in CPT1 can cause carnitine palmitoyltransferase I (CPT I) deficiency, which is an autosomal recessive genetic condition (need two copies of the mutation)

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The total score was 12

Genet Mol Res 10(1):419428 Siju S, Dhanya K, Syamkumar S, Sasikumar B, Sheeja TE, Bhat AI, Parthasarathy VA (2010a) Development, characterization and cross species amplification of polymorphic microsatellite markers from expressed sequence tags of turmeric ( Curcuma longa L.)