Course of Selenoprotein-Related Myopathies
The clinical course and genotype-phenotype correlations in 41 patients aged 1-60 years with selenoprotein-related myopathy (SEPNRM) due to SEPN1 gene mutations were evaluated retrospectively in a study at The Dubowitz Neuromuscular Center, London, and other centers in the UK.
Furkejuvvon:
| Váldodahkki: | |
|---|---|
| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
Pediatric Neurology Briefs Publishers
2011-08-01
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| Ráidu: | Pediatric Neurology Briefs |
| Fáttát: | |
| Liŋkkat: | https://www.pediatricneurologybriefs.com/articles/664 |
| Fáddágilkorat: |
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