Caspase-dependent apoptosis in Riboflavin Transporter Deficiency iPSCs and derived motor neurons
Abstract Riboflavin Transporter Deficiency (RTD) is a rare genetic, childhood-onset disease. This pathology has a relevant neurological involvement, being characterized by motor symptoms, ponto-bulbar paralysis and sensorineural deafness. Such clinical presentation is associated with muscle weakness...
Kaydedildi:
| Asıl Yazarlar: | , , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Nature Publishing Group
2024-01-01
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| Seri Bilgileri: | Cell Death Discovery |
| Online Erişim: | https://doi.org/10.1038/s41420-024-01812-y |
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