The Function of Survival Motor Neuron Complex and Its Role in Spinal Muscular Atrophy Pathogenesis - ScienceDirect
Reduced Survival of Motor Neuron (SMN) Protein in Motor Neuronal Progenitors Functions Cell Autonomously to Cause Spinal Muscular Atrophy in Model Mice Expressing the Human Centromeric (SMN2) Gene | Journal of Neuroscience
SMA Awareness Month 1: What is SMA? – Bilkent UNAM iGEM Team
Spinal Muscular Atrophy Causes
Copy Number Variations in the Survival Motor Neuron Genes: Implications for Spinal Muscular Atrophy and Other Neurodegenerative Diseases | Semantic Scholar
IJMS | Free Full-Text | Genomic Variability in the Survival Motor Neuron Genes (SMN1 and SMN2): Implications for Spinal Muscular Atrophy Phenotype and Therapeutics Development
Converging Mechanisms of p53 Activation Drive Motor Neuron Degeneration in Spinal Muscular Atrophy - ScienceDirect
Biogen on X: "#SMA is caused by a mutation in the survival motor neuron 1 (SMN1) gene, which maintains the health and normal function of motor neurons. https://t.co/uUdVjujm9P" / X
Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick? | Nature Reviews Neuroscience
Survival of motor neuron - Wikipedia
Is Good Housekeeping the Key to Motor Neuron Survival?: Cell
Cell type diversity of requirement for survival motor neuron | Download Scientific Diagram
Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick? | Nature Reviews Neuroscience
JCM | Free Full-Text | New Treatments in Spinal Muscular Atrophy: Positive Results and New Challenges
Diverse role of survival motor neuron protein - ScienceDirect
IJMS | Free Full-Text | Regulation of Survival Motor Neuron Gene Expression by Calcium Signaling
Advances and limitations for the treatment of spinal muscular atrophy | BMC Pediatrics | Full Text
Spinal Muscular Atrophy: Causes, Symptoms Of This Genetic Disorder With World's Most Expensive Drug
Spinal Muscular Atrophy Pathophysiology - Rare Disease Advisor
![PDF] Genomic Variability in the Survival Motor Neuron Genes (SMN1 and SMN2): Implications for Spinal Muscular Atrophy Phenotype and Therapeutics Development | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/e390febd3fb064f09c54d6166c7a143bbb17953b/5-Figure2-1.png "PDF] Genomic Variability in the Survival Motor Neuron Genes (SMN1 and SMN2): Implications for Spinal Muscular Atrophy Phenotype and Therapeutics Development | Semantic Scholar")
PDF] Genomic Variability in the Survival Motor Neuron Genes (SMN1 and SMN2): Implications for Spinal Muscular Atrophy Phenotype and Therapeutics Development | Semantic Scholar
Frontiers | The Need for SMN-Independent Treatments of Spinal Muscular Atrophy (SMA) to Complement SMN-Enhancing Drugs
The survival of motor neuron gene (SMN) consists of 9 exons, with the... | Download Scientific Diagram
Treatment for Spinal Muscular Atrophy Using Onasemnogene Abeparvovec - touchNEUROLOGY
The role of survival motor neuron protein (SMN) in protein homeostasis | Cellular and Molecular Life Sciences
Therapy development for spinal muscular atrophy: perspectives for muscular dystrophies and neurodegenerative disorders | Neurological Research and Practice | Full Text
Spinal Muscular Atrophy as a Treatable Disease: Disease-Modifying Therapies Improving Clinical Outcomes and Quality of Life - Neurology Advisor
Survival Motor Neuron Protein 1 - an overview | ScienceDirect Topics
