Spinal muscular atrophy—clinical and genetic correlations
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Cited by 101 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Motor patterns of patients with spinal muscular atrophy suggestive of sensory and corticospinal contributions to the development of locomotor muscle synergies;Journal of Neurophysiology;2024-02-01
2. Establishment of a Pilot Newborn Screening Program for Spinal Muscular Atrophy in Saint Petersburg;International Journal of Neonatal Screening;2024-01-25
3. Assessment of Nuclear Gem Quantity for Evaluating the Efficacy of Antisense Oligonucleotides in Spinal Muscular Atrophy Cells;Methods and Protocols;2024-01-19
4. Deep Molecular Characterization of Milder Spinal Muscular Atrophy Patients Carrying the c.859G>C Variant in SMN2;International Journal of Molecular Sciences;2022-07-27
5. Bap1/SMN axis in Dpp4+ skeletal muscle mesenchymal cells regulates the neuromuscular system;JCI Insight;2022-05-23
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