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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Vydáno v:BMC Genomics
Hlavní autoři: 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.
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2016
Témata:
Research
On-line přístup: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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