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A303 GASTROINTESTINAL MANIFESTATIONS IN PATIENTS WITH CONGENITAL MYOTONIC DYSTROPHY
BACKGROUND: Myotonic Dystrophy type 1 is an autosomal dominant, multisystem disease characterized by muscle weakness and myotonia. Phenotypes include congenital, childhood and classic adult onset. Congenital Myotonic Dystrophy (CDM) is the most severe occurring in neonates, characterized by severe h...
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| 出版年: | J Can Assoc Gastroenterol |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6508232/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jcag/gwy009.303 |
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