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SLC6A14, an amino acid transporter, modifies the primary CF defect in fluid secretion
The severity of intestinal disease associated with Cystic Fibrosis (CF) is variable in the patient population and this variability is partially conferred by the influence of modifier genes. Genome-wide association studies have identified SLC6A14, an electrogenic amino acid transporter, as a genetic...
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| Publicado no: | eLife |
|---|---|
| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
eLife Sciences Publications, Ltd
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6054531/ https://ncbi.nlm.nih.gov/pubmed/30004386 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7554/eLife.37963 |
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