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Genetic variations within the OPA1 gene are not associated with neuromyelitis optica
Neuromyelitis optica (NMO) is an idiopathic demyelinating disease which predominantly affects the optic nerve and spinal cord. Multiplex NMO pedigrees have been reported but the genetic risk factors conferring this increased familial susceptibility have not yet been determined. OPA1 mutations have r...
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| Asıl Yazarlar: | , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2011
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4040403/ https://ncbi.nlm.nih.gov/pubmed/21828197 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1352458511416838 |
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