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Huntington Disease as a Neurodevelopmental Disorder and Early Signs of the Disease in Stem Cells
Huntington disease (HD) is a dominantly inherited disorder caused by a CAG expansion mutation in the huntingtin (HTT) gene, which results in the HTT protein that contains an expanded polyglutamine tract. The adult form of HD exhibits a late onset of the fully symptomatic phase. However, there is als...
שמור ב:
| הוצא לאור ב: | Mol Neurobiol |
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| Main Authors: | , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Springer US
2017
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5842500/ https://ncbi.nlm.nih.gov/pubmed/28497201 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12035-017-0477-7 |
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