Načítá se...
The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption
The proton-coupled folate transporter (PCFT) is the mechanism by which folates are absorbed across the apical brush-border membrane of the small intestine. The transporter is also expressed in the choroid plexus and is required for transport of folates into the cerebrospinal fluid. Loss of PCFT func...
Uloženo v:
| Vydáno v: | Mol Aspects Med |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2016
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5253092/ https://ncbi.nlm.nih.gov/pubmed/27664775 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mam.2016.09.002 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|