Personalized Treatment for Infantile Ascending Hereditary Spastic Paralysis Based on In Silico Strategies

Infantile onset hereditary spastic paralysis (IAHSP) is a rare neurological disease diagnosed in less than 50 children worldwide. It is transmitted with a recessive pattern and originates from mutations of the ALS2 gene, encoding for the protein alsin and involved in differentiation and maintenance...

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Detalles Bibliográficos
Autores principales: Rossi Sebastiano, Matteo, Ermondi, Giuseppe, Sato, Kai, Otomo, Asako, Hadano, Shinji, Caron, Giulia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9609931/
https://www.ncbi.nlm.nih.gov/pubmed/36296656
http://dx.doi.org/10.3390/molecules27207063

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9609931/
https://www.ncbi.nlm.nih.gov/pubmed/36296656
http://dx.doi.org/10.3390/molecules27207063

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