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Genetic diagnosis as a tool for personalized treatment of Duchenne muscular dystrophy
Accurate definition of genetic mutations causing Duchenne muscular dystrophy (DMD) has always been relevant in order to provide genetic counseling to patients and families, and helps to establish the prognosis in the case where the distinction between Duchenne, Becker, or intermediate muscular dystr...
Tallennettuna:
| Julkaisussa: | Acta Myol |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Pacini Editore SRL
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5416739/ https://ncbi.nlm.nih.gov/pubmed/28484312 |
| Tagit: |
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