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Patient Input to Inform the Development of Central Nervous System Outcome Measures in Myotonic Dystrophy
Myotonic dystrophy type 1 (DM1) and myotonic dystrophy type 2 (DM2) are multisystem, genetic disorders caused by repeat expansions on chromosome 19 (DM1) and chromosome 3 (DM2). Although the effects of DM on the skeletal, cardiac, and smooth muscles, as well as the endocrine and central nervous syst...
保存先:
| 出版年: | Ther Innov Regul Sci |
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| 第一著者: | |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Springer International Publishing
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7458891/ https://ncbi.nlm.nih.gov/pubmed/31970692 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s43441-020-00117-3 |
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