CTG-Repeat Detection in Primary Human Myoblasts of Myotonic Dystrophy Type 1
Myotonic dystrophy type 1 (DM1) is an autosomal dominant multisystemic disorder caused by unstable CTG-repeat expansions in the DMPK gene. Tissue mosaicism has been described for the length of these repeat expansions. The most obvious affected tissue is skeletal muscle, making it the first target fo...
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| Principais autores: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2021-06-01
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| Colecção: | Frontiers in Neuroscience |
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| Acesso em linha: | https://www.frontiersin.org/articles/10.3389/fnins.2021.686735/full |
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