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Drug Screening and Drug Repositioning as Promising Therapeutic Approaches for Spinal Muscular Atrophy Treatment

Spinal muscular atrophy (SMA) is the most common genetic disease affecting infants and young adults. Due to mutation/deletion of the survival motor neuron (SMN) gene, SMA is characterized by the SMN protein lack, resulting in motor neuron impairment, skeletal muscle atrophy and premature death. Even...

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Bibliografski detalji
Izdano u:Front Pharmacol
Glavni autori: Menduti, Giovanna, Rasà, Daniela Maria, Stanga, Serena, Boido, Marina
Format: Artigo
Jezik:Inglês
Izdano: Frontiers Media S.A. 2020
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7689316/
https://ncbi.nlm.nih.gov/pubmed/33281605
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphar.2020.592234
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