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Phenotypic variability of a likely FA2H founder mutation in a family with complicated hereditary spastic paraplegia
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| 發表在: | Clin Genet |
|---|---|
| Main Authors: | , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2013
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5030767/ https://ncbi.nlm.nih.gov/pubmed/23745665 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cge.12185 |
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