Myotonic dystrophy: genetics and clinical polymorphism
Myotonic dystrophy is the most common form of hereditary progressive muscular dystrophy in adults. The disorder is characterized by progressive course, autosomal dominant inheritance and multisystem involvement (skeletal muscles, myocardium, endocrine system, eyes, etc.). The paper highlights a huge...
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| Autores principales: | , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Research Center of Neurology
2019-03-01
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| Colección: | Анналы клинической и экспериментальной неврологии |
| Materias: | |
| Acceso en línea: | https://annaly-nevrologii.com/journal/pathID/article/viewFile/574/461 |
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