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...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:BMC Genomics
Κύριοι συγγραφείς: 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.
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: BioMed Central 2016
Θέματα:
Research
Διαθέσιμο Online: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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