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Neuronal intranuclear inclusion disease is genetically heterogeneous
Neuronal intranuclear inclusion disease (NIID) is a clinically heterogeneous neurodegenerative condition characterized by pathological intranuclear eosinophilic inclusions. A CGG repeat expansion in NOTCH2NLC was recently identified to be associated with NIID in patients of Japanese descent. We scre...
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| Udgivet i: | Ann Clin Transl Neurol |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
John Wiley and Sons Inc.
2020
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7480908/ https://ncbi.nlm.nih.gov/pubmed/32777174 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.51151 |
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