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Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia
Hereditary ataxia and spastic paraplegia are heterogeneous monogenic neurodegenerative disorders. To date, a large number of individuals with such disorders remain undiagnosed. Here, we have assessed molecular diagnosis by gene panel sequencing in 105 early and late-onset hereditary ataxia and spast...
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| 出版年: | PLoS One |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Public Library of Science
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5375131/ https://ncbi.nlm.nih.gov/pubmed/28362824 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0174667 |
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