Spinocerebellar ataxia 27B: A novel, frequent and potentially treatable ataxia
Abstract Hereditary ataxias, especially when presenting sporadically in adulthood, present a particular diagnostic challenge owing to their great clinical and genetic heterogeneity. Currently, up to 75% of such patients remain without a genetic diagnosis. In an era of emerging disease‐modifying gene...
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| Hlavní autoři: | , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Wiley
2024-01-01
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| Edice: | Clinical and Translational Medicine |
| Témata: | |
| On-line přístup: | https://doi.org/10.1002/ctm2.1504 |
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