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Molecular diagnosis of patients with epilepsy and developmental delay using a customized panel of epilepsy genes
Pediatric epilepsies are a group of disorders with a broad phenotypic spectrum that are associated with great genetic heterogeneity, thus making sequential single-gene testing an impractical basis for diagnostic strategy. The advent of next-generation sequencing has increased the success rate of epi...
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| Publicado no: | PLoS One |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5708701/ https://ncbi.nlm.nih.gov/pubmed/29190809 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0188978 |
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