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...

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Detalles Bibliográficos
Autores principales: Jensen, Nina, Autzen, Jacob Kwasi, Pedersen, Lene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Short Communication
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

Internet

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

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