Cutaneous findings in myotonic dystrophyCapsule Summary
Myotonic dystrophy types 1 and 2 are a group of complex genetic disorders resulting from the expansion of (CTG)n nucleotide repeats in the DMPK gene. In addition to the hallmark manifestations of myotonia and skeletal muscle atrophy, myotonic dystrophy also affects a myriad of other organs including...
| Päätekijät: | , |
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| Aineistotyyppi: | Artikkeli |
| Kieli: | English |
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Elsevier
2022-06-01
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| Sarja: | JAAD International |
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| Linkit: | http://www.sciencedirect.com/science/article/pii/S2666328721000778 |