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A Case of Myotonic Dystrophy with Electrolyte Imbalance
Type 1 myotonic dystrophy (DM1) is an autosomal-dominant inherited disorder with a multisystem involvement, caused by an abnormal expansion of the CTG sequence of the dystrophic myotonia protein kinase (DMPK) gene. DM1 is a variable multisystem disorder with muscular and nonmuscular abnormalities. I...
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| 主要な著者: | , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
The Korean Academy of Medical Sciences
2013
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3708088/ https://ncbi.nlm.nih.gov/pubmed/23853500 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3346/jkms.2013.28.7.1111 |
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