Fingerprint
Dive into the research topics of 'Mutation of the proton-coupled folate transporter gene (PCFT-SLC46A1) in Turkish siblings with hereditary folate malabsorption'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
Mutation of the proton-coupled folate transporter gene (PCFT-SLC46A1) in Turkish siblings with hereditary folate malabsorption
Berna Atabay, Meral Turker, Esra Arun Ozer, Kris Mahadeo, Ndeye Diop-Bove, I. David Goldman
Research output: Contribution to journal › Article › peer-review
25
Scopus
citations