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                                       Details for article 29 of 53 found articles
 
 
  Prevalence of a Loss-of-Function Mutation in the Proton-Coupled Folate Transporter Gene (PCFT-SLC46A1) Causing Hereditary Folate Malabsorption in Puerto Rico
 
 
Title: Prevalence of a Loss-of-Function Mutation in the Proton-Coupled Folate Transporter Gene (PCFT-SLC46A1) Causing Hereditary Folate Malabsorption in Puerto Rico
Author: Mahadeo, Kris M.
Diop-Bove, Ndeye
Ramirez, Sonia I.
Cadilla, Carmen L.
Rivera, Enid
Martin, Madelena
Lerner, Norma B.
DiAntonio, Lisa
Duva, Salvatore
Santiago-Borrero, Pedro J.
Goldman, I. David
Appeared in: Journal of pediatrics
Paging: Volume 159 (2011) nr. 4 pages 5648 p.
Year: 2011
Contents:
Publisher: Mosby, Inc.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 29 of 53 found articles
 
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