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Autor:
Mariana RAMOS-BROSSIER, David ROMEO-GUITART, Fabien LANTE, Valerie Boitez, François MAILLIET, Sohame SAHA, Manon RIVAGORDA, Eleni SIOPI, Ivan Namazanyy, Leroy Christine, Stéphanie Moriceau, Sarah BECK-CORMIER, Patrice Codogno, Alain BUISSON, Laurent BECK, Gerard Friedlander, Franck Oury
In recent years, primary familial brain calcification (PFBC), a rare neurological disease characterized by a wide spectrum of cognitive disorders, has been associated to mutations in the sodium (Na)-Phosphate (Pi) co-transporter SLC20A2. However, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::159ed62f10b94f4f626fe9278e49c520
https://doi.org/10.21203/rs.3.rs-2727315/v1
https://doi.org/10.21203/rs.3.rs-2727315/v1