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Clinical utility of multigene analysis in over 25,000 patients with neuromuscular disorders
OBJECTIVE: Molecular genetic testing for hereditary neuromuscular disorders is increasingly used to identify disease subtypes, determine prevalence, and inform management and prognosis, and although many small disease-specific studies have demonstrated the utility of genetic testing, comprehensive d...
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| Publicado no: | Neurol Genet |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7164976/ https://ncbi.nlm.nih.gov/pubmed/32337338 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000412 |
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