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Recent Overview of the Use of iPSCs Huntington’s Disease Modeling and Therapy
Huntington’s disease (HD) is an inherited, autosomal dominant, degenerative disease characterized by involuntary movements, cognitive decline, and behavioral impairment ending in death. HD is caused by an expansion in the number of CAG repeats in the huntingtin gene on chromosome 4. To date, no effe...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7139425/ https://www.ncbi.nlm.nih.gov/pubmed/32213859 http://dx.doi.org/10.3390/ijms21062239 |