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Phenotypic variability of a likely FA2H founder mutation in a family with complicated hereditary spastic paraplegia
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| Udgivet i: | Clin Genet |
|---|---|
| Main Authors: | , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2013
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| Fag: | |
| Online adgang: | 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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