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The orphan solute carrier SLC10A7 is a novel negative regulator of intracellular calcium signaling
SLC10A7 represents an orphan member of the Solute Carrier Family SLC10. Recently, mutations in the human SLC10A7 gene were associated with skeletal dysplasia, amelogenesis imperfecta, and decreased bone mineral density. However, the exact molecular function of SLC10A7 and the mechanisms underlying t...
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| Publicat a: | Sci Rep |
|---|---|
| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group UK
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7190670/ https://ncbi.nlm.nih.gov/pubmed/32350310 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-020-64006-3 |
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