Učitavanje...

Nusinersen: A Novel Antisense Oligonucleotide for the Treatment of Spinal Muscular Atrophy

Spinal muscular atrophy (SMA) encompasses a group of autosomal recessively inherited degenerative neuromuscular disorders. They range in severity from neonatal onset with rapidly progressive weakness and early mortality (SMA-1), to onset in infancy (SMA-2), to adolescent/adult onset with indolent cl...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Izdano u:J Pediatr Pharmacol Ther
Glavni autori: Neil, Erin E., Bisaccia, Elizabeth K.
Format: Artigo
Jezik:Inglês
Izdano: Pediatric Pharmacy Advocacy Group 2019
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6510522/
https://ncbi.nlm.nih.gov/pubmed/31093018
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5863/1551-6776-24.3.194
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!