SMN, the product of the spinal muscular atrophy-determining gene, is expressed widely but selectively in the developing human forebrain
Author:
Publisher
Wiley
Subject
General Neuroscience
Reference47 articles.
1. Neuropathological analysis in spinal muscular atrophy type II
2. Expression of the SMN Gene, the Spinal Muscular Atrophy Determining Gene, in the Mammalian Central Nervous System
3. Subcellular distribution of survival motor neuron (SMN) protein: possible involvement in nucleocytoplasmic and dendritic transport
4. Is spinal muscular atrophy the result of defects in motor neuron processes?
5. The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophy
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1. Cognitive function in SMA patients with 2 or 3 SMN2 copies treated with SMN-modifying or gene addition therapy during the first year of life;European Journal of Paediatric Neurology;2024-07
2. Impaired Neurodevelopment in Children with 5q-SMA - 2 Years After Newborn Screening;Journal of Neuromuscular Diseases;2024-01-02
3. Sleep architecture and Nusinersen therapy in children with Spinal Muscular Atrophy type 1;Sleep Medicine;2023-10
4. Brain Magnetic Resonance Imaging (MRI) in Spinal Muscular Atrophy: A Scoping Review;Journal of Neuromuscular Diseases;2023-07-04
5. Cognitive performance of adult patients with SMA before and after treatment initiation with nusinersen;BMC Neurology;2023-06-06
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