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Copy number variations in Saudi family with intellectual disability and epilepsy
BACKGROUND: Epilepsy is genetically complex but common brain disorder of the world affecting millions of people with almost of all age groups. Novel Copy number variations (CNVs) are considered as important reason for the numerous neurodevelopmental disorders along with intellectual disability and e...
Guardado en:
| Publicado en: | BMC Genomics |
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| Autores principales: | , , , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BioMed Central
2016
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5073808/ https://ncbi.nlm.nih.gov/pubmed/27766957 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-016-3091-6 |
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