Molecular Pathophysiological Mechanisms in Huntington’s Disease
Huntington’s disease is an inherited neurodegenerative disease described 150 years ago by George Huntington. The genetic defect was identified in 1993 to be an expanded CAG repeat on exon 1 of the huntingtin gene located on chromosome 4. In the following almost 30 years, a considerable amount of res...
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| Natura: | Artigo |
| Lingua: | Inglês |
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MDPI AG
2022-06-01
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| Serie: | Biomedicines |
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| Accesso online: | https://www.mdpi.com/2227-9059/10/6/1432 |
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