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Prenatal diagnosis for a Chinese family with a de novo DMD gene mutation: A case report
BACKGROUND: Patients with Duchenne muscular dystrophy (DMD) usually have severe and fatal symptoms. At present, there is no effective treatment for DMD, thus it is very important to avoid the birth of children with DMD by effective prenatal diagnosis. We identified a de novo DMD gene mutation in a C...
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| Publicat a: | Medicine (Baltimore) |
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| Autors principals: | , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Wolters Kluwer Health
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5815683/ https://ncbi.nlm.nih.gov/pubmed/29390271 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000008814 |
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