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Mutations in Folate Transporter Genes and Risk for Human Myelomeningocele
The molecular mechanisms linking folate deficiency and neural tube defect (NTD) risk in offspring remain unclear. Folate transporters (SLC19A1, SLC46A1, SLC25A32, and FOLH1) and folate receptors (FOLR1, FOLR2, and FOLR3) are suggested to play essential roles in transporting folate from maternal inte...
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| Publicado no: | Am J Med Genet A |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5650522/ https://ncbi.nlm.nih.gov/pubmed/28948692 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.38472 |
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