Homozygous R136S mutation in PRNP gene causes inherited early onset prion disease

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Bibliographic Details
Main Authors: Ximelis, Teresa, Marín-Moreno, Alba, Espinosa Martín, Juan Carlos, Eraña, Hasier, Charco, Jorge M., Hernández, Isabel, Riveira, Carmen, Alcolea, Daniel, González-Roca, Eva, Aldecoa, Iban, Molina-Porcel, Laura, Parchi, Piero, Rossi, Marcello, Castilla, Joaquín, Ruiz-García, Raquel, Gelpi, Ellen, Torres, Juan María, Sánchez-Valle, Raquel
Other Authors: Instituto de Salud Carlos III
Format: artículo biblioteca
Language:English
Published: Springer Nature 2021-10-18
Subjects:GSS, Gene PRNP, Homozygous, Neuropathology, Prion,
Online Access:http://hdl.handle.net/10261/281188
http://dx.doi.org/10.13039/501100004837
http://dx.doi.org/10.13039/501100004587
http://dx.doi.org/10.13039/100008666
https://api.elsevier.com/content/abstract/scopus_id/85117480580
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