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[DOI] [PMC free article] [PubMed] [Google Scholar] Park J, Look KA, 2019
10.1038/nn.2736 Nat

Hereditary basis: Primary carnitine deficiency is transmitted as an autosomal recessive disorder caused by mutations in the SLC22A5 gene on 5q31.1

Associative learning was assessed using an automated fear conditioning system for mice (Coulbourn Instruments, Allentown, PA) with the following parameters: Day 1, acquisition: three min habituation to context A, followed by two tone (80 dB) and 0.5 mA footshock pairings