[Hereditary folate malabsorption due to an SLC46A1 mutation with cerebral folate deficiency and refractory epilepsy: first case reported in Argentina].
Overview & Synopsis
Open access biomedical research article published in Rev Fac Cien Med Univ Nac Cordoba.
Indexed from repository: PubMed Central
(
pmc.ncbi.nlm.nih.gov)
Keyboard Shortcuts:
← / → for pages • + / - for zoom • 0 to fit width
Powered by Mozilla PDF.js v3.11
Document Information
| Document Title | [Hereditary folate malabsorption due to an SLC46A1 mutation with cerebral folate deficiency and refractory epilepsy: first case reported in Argentina]. |
|---|---|
| Author / Organization | Grosso CL, Peralta LV, Paviolo M, Pautasso J, Guelbert GA, Bovina Martijena MDP, Laróvere LE |
| Subject & Discipline | Rev Fac Cien Med Univ Nac Cordoba |
| Categories | Medicine & Health |
| Publication Year | 2026 |
| License / Rights | Open Access / Creative Commons |
| Resource Verification | Listed PDF (Verification Pending) |
| Original Host Website |
PubMed Central
(pmc.ncbi.nlm.nih.gov)
|
| File Format | application/pdf (Portable Document Format) |
| Language | EN |
| Catalog ID | DOC-140256 |
| Original Source Link | Visit Source Page on pmc.ncbi.nlm.nih.gov » |