Establishment of mouse model of inherited PIGO deficiency and therapeutic potential of AAV-based gene therapy

Inherited glycosylphosphatidylinositol (GPI) deficiency (IGD) is caused by mutations in GPI biosynthesis genes. The mechanisms of its systemic, especially neurological, symptoms are not clarified and fundamental therapy has not been established. Here, we report establishment of mouse models of IGD c...

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Detalles Bibliográficos
Autores principales: Kuwayama, Ryoko, Suzuki, Keiichiro, Nakamura, Jun, Aizawa, Emi, Yoshioka, Yoshichika, Ikawa, Masahito, Nabatame, Shin, Inoue, Ken-ichi, Shimmyo, Yoshiari, Ozono, Keiichi, Kinoshita, Taroh, Murakami, Yoshiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166810/
https://www.ncbi.nlm.nih.gov/pubmed/35661110
http://dx.doi.org/10.1038/s41467-022-30847-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166810/
https://www.ncbi.nlm.nih.gov/pubmed/35661110
http://dx.doi.org/10.1038/s41467-022-30847-x

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