Longitudinal Transcriptomic Analysis Reveals Systemic Effects of Risdiplam in Adults with Spinal Muscular Atrophy

Background: Spinal Muscular Atrophy (SMA) is a neurodegenerative disease caused by reduced survival motor neuron (SMN) protein levels due to <i>SMN1</i> gene mutations. The natural history of SMA has dramatically changed since innovative therapies were approved; among them, Risdiplam (an oral molecu...

وصف كامل

التفاصيل البيبلوغرافية

المؤلفون الرئيسيون:	Maria Liguori, Arianna Consiglio, Eustachio D’Errico, Ylenia Antonacci, Martina Coffa, Alessandro Introna, Isabella Laura Simone
التنسيق:	Artigo
اللغة:	Inglês
منشور في:	MDPI AG 2026-06-01
سلاسل:	Brain Sciences
الموضوعات:	spinal muscular atrophy Risdiplam Transcriptomics <i>SMN2</i> gene RNA sequencing
الوصول للمادة أونلاين:	https://www.mdpi.com/2076-3425/16/6/643
الوسوم:	إضافة وسم لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!