Pagliarini et al., 2020 - Google Patents
Combined treatment with the histone deacetylase inhibitor LBH589 and a splice‐switch antisense oligonucleotide enhances SMN2 splicing and SMN expression in …Pagliarini et al., 2020
- Document ID
- 4370469799473454259
- Author
- Pagliarini V
- Guerra M
- Di Rosa V
- Compagnucci C
- Sette C
- Publication year
- Publication venue
- Journal of Neurochemistry
External Links
Snippet
Spinal muscular atrophy (SMA) is a motor neuron disease caused by loss of function mutations in the Survival Motor Neuron 1 (SMN1) gene and reduced expression of the SMN protein, leading to spinal motor neuron death, muscle weakness and atrophy. Although …
- 208000002320 Spinal Muscular Atrophy 0 title abstract description 125
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