Genome wide analysis of novel copy number variations duplications/deletions of different epileptic patients in Saudi Arabia

BACKGROUND: Epilepsy is genetically complex neurological disorder affecting millions of people of different age groups varying in its type and severity. Copy number variants (CNVs) are key players in the genetic etiology of numerous neurodevelopmental disorders and prior findings also revealed that...

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Bibliografische gegevens
Gepubliceerd in:BMC Genomics
Hoofdauteurs: Naseer, Muhammad Imran, Faheem, Muhammad, Chaudhary, Adeel G, Kumosani, Taha A, Al-Quaiti, Maha Mohsin, Jan, Mohammed M, Saleh Jamal, Hasan, Al-Qahtani, Mohammad H
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2015
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Research
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4315149/
https://ncbi.nlm.nih.gov/pubmed/25923336
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-16-S1-S10
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