Course of Selenoprotein-Related Myopathies
Abstract
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.
DOI: https://doi.org/10.15844/pedneurbriefs-25-8-10 | Journal eISSN: 2166-6482
Language: English
Page range: 64 - 64
Published on: Aug 1, 2011
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 2011 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.