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A Nonredundant Role for the TRPM6 Channel in Neural Tube Closure
In humans, germline mutations in Trpm6 cause autosomal dominant hypomagnesemia with secondary hypocalcemia disorder. Loss of Trpm6 in mice also perturbs cellular magnesium homeostasis but additionally results in early embryonic lethality and neural tube closure defects. To define the mechanisms by w...
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| Publicat a: | Sci Rep |
|---|---|
| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group UK
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5688082/ https://ncbi.nlm.nih.gov/pubmed/29142255 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-15855-y |
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