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Slc20a2 is critical for maintaining a physiologic inorganic phosphate level in cerebrospinal fluid
Mutations in the SLC20A2-gene encoding the inorganic phosphate (Pi) transporter PiT2 can explain approximately 40 % of the familial cases of the rare neurodegenerative disorder primary familial brain calcification (Fahr’s disease). The disease characteristic, cerebrovascular-associated calcification...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer Berlin Heidelberg
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4794525/ https://www.ncbi.nlm.nih.gov/pubmed/26660102 http://dx.doi.org/10.1007/s10048-015-0469-6 |