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GNE genotype explains 20% of phenotypic variability in GNE myopathy
OBJECTIVE: To test the hypothesis that common GNE mutations influence disease severity; using statistical analysis of patient cohorts from different countries. METHODS: Systematic literature review identified 11 articles reporting 759 patients. GNE registry data were used as a second data set. The r...
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| Publicado en: | Neurol Genet |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Wolters Kluwer
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6384023/ https://ncbi.nlm.nih.gov/pubmed/30842975 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000308 |
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