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Repeat expansion scanning of the NOTCH2NLC gene in patients with multiple system atrophy
OBJECTIVE: Trinucleotide GGC repeat expansion in the 5’UTR of the NOTCH2NLC gene has been recognized as the pathogenesis of neuronal intranuclear inclusion disease (NIID). Previous studies have described that some NIID patients showed clinical and pathological similarities with multiple system atrop...
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| Izdano u: | Ann Clin Transl Neurol |
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| Glavni autori: | , , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
John Wiley and Sons Inc.
2020
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7187708/ https://ncbi.nlm.nih.gov/pubmed/32250060 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.51021 |
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