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Screening for REEP1 Mutations in 31 Chinese Hereditary Spastic Paraplegia Families
Background: REEP1 is a common cause of autosomal dominant hereditary spastic paraplegia (HSP) but is rare in China. The pathological mechanism of REEP1 is not fully understood. Methods: We screened for REEP1 mutations in 31 unrelated probands from Chinese HSP families using next-generation sequencin...
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| I publikationen: | Front Neurol |
|---|---|
| Huvudupphovsmän: | , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Frontiers Media S.A.
2020
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7325443/ https://ncbi.nlm.nih.gov/pubmed/32655478 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2020.00499 |
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