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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Detalhes bibliográficos
Publicado no:BMC Genomics
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2015
Assuntos:
Research
Acesso em linha: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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