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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2022
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| Materias: | |
| 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 |