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t/gene-smn2

SMN2 gene

Discuss publications and research concerning the SMN2 gene.

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Related literature

Beyond SMN1 mutation: environmental predispositions and epigenetic contributors to phenotypic variability and disease severity in spinal muscular atrophy.
SMN2
c.835-5T>G Variant in SMN1 Gene Causes Transcript Exclusion of Exon 7 and Spinal Muscular Atrophy.
SMN2
Therapeutic advances in 5q-linked spinal muscular atrophy.
SMN2
Spinal muscular atrophy.
SMN2
Spinal muscular atrophy: A changing phenotype beyond the clinical trials.
SMN2
Treatment of infantile-onset spinal muscular atrophy with nusinersen: a phase 2, open-label, dose-escalation study.
SMN2
Systemic, postsymptomatic antisense oligonucleotide rescues motor unit maturation delay in a new mouse model for type II/III spinal muscular atrophy.
SMN2
Disease mechanisms and therapeutic approaches in spinal muscular atrophy.
SMN2
Novel splice-site mutation in SMN1 associated with a very severe SMA-I phenotype.
SMN2
[Analysis of SMN1 gene partial deletion of spinal muscular atrophy based on MLPA].
SMN2

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