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7. Prevalence of a loss-of-function mutation in the proton-coupled folate transporter gene (PCFT-SLC46A1) causing hereditary folate malabsorption in Puerto Rico. Mahadeo KM; Diop-Bove N; Ramirez SI; Cadilla CL; Rivera E; Martin M; Lerner NB; DiAntonio L; Duva S; Santiago-Borrero PJ; Goldman ID J Pediatr; 2011 Oct; 159(4):623-7.e1. PubMed ID: 21489556 [TBL] [Abstract][Full Text] [Related]
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14. An ancestry informative marker panel design for individual ancestry estimation of Hispanic population using whole exome sequencing data. Wang LJ; Zhang CW; Su SC; Chen HH; Chiu YC; Lai Z; Bouamar H; Ramirez AG; Cigarroa FG; Sun LZ; Chen Y BMC Genomics; 2019 Dec; 20(Suppl 12):1007. PubMed ID: 31888480 [TBL] [Abstract][Full Text] [Related]
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18. Frequency and clinicopathological characteristics of presenilin 1 Gly206Ala mutation in Puerto Rican Hispanics with dementia. Arnold SE; Vega IE; Karlawish JH; Wolk DA; Nunez J; Negron M; Xie SX; Wang LS; Dubroff JG; McCarty-Wood E; Trojanowski JQ; Van Deerlin V J Alzheimers Dis; 2013; 33(4):1089-95. PubMed ID: 23114514 [TBL] [Abstract][Full Text] [Related]
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