Rare DMD Gene Duplication in a Lebanese Child With Duchene Muscular Dystrophy
ABSTRACT A five‐year‐old boy with clinical features of Duchenne muscular dystrophy was found to have a rare de novo DMD exon 2–9 duplication. Reporting such atypical duplications improves genotype–phenotype interpretation and highlights the need for multidisciplinary care, particularly in resource‐l...
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| 主要な著者: | , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Wiley
2026-02-01
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| シリーズ: | Clinical Case Reports |
| 主題: | |
| オンライン･アクセス: | https://doi.org/10.1002/ccr3.71967 |
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