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...

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Detalhes bibliográficos
Publicado no:BMC Genomics
Main Authors: Naseer, Muhammad I., Chaudhary, Adeel G., Rasool, Mahmood, Kalamegam, Gauthaman, Ashgan, Fai T., Assidi, Mourad, Ahmed, Farid, Ansari, Shakeel A., Zaidi, Syed Kashif, Jan, Mohammed M., Al-Qahtani, Mohammad H.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2016
Assuntos:
Research
Acesso em linha: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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