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Clinical and Pathological Features of Korean Patients with DNM2-Related Centronuclear Myopathy
BACKGROUND AND PURPOSE: Centronuclear myopathy (CNM) is characterized by the presence of central nuclei within a large number of muscle fibers. Mutations of the dynamin 2 gene (DNM2) are common causes of autosomal dominant or sporadic CNM. The aim of this study was to characterize the clinical and p...
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| Main Authors: | , , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Korean Neurological Association
2014
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3896645/ https://ncbi.nlm.nih.gov/pubmed/24465259 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3988/jcn.2014.10.1.24 |
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