Prevalence of a loss-of-function mutation in the proton-coupled folate transporter gene (PCFT-SLC46A1) causing hereditary folate malabsorption in Puerto Rico

Kris M. Mahadeo, Ndeye Diop-Bove, Sonia I. Ramirez, Carmen L. Cadilla, Enid Rivera, Madelena Martin, Norma B. Lerner, Lisa Diantonio, Salvatore Duva, Pedro J. Santiago-Borrero, I. David Goldman

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