Search Results - Diop-Bove, N.

  • Showing 1 - 1 results of 1
Refine Results
  1. 1
    A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorption

    A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorption by Diop-Bove, N., Jain, M., Scaglia, F., Goldman, I.D.

    Published in Gene
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:

Search Tools: