Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8758835 | Journal of the Chinese Medical Association | 2018 | 5 Pages |
Abstract
A silent mutation was identified at locus 27,909Â CÂ >Â T in 30.66% of the total screened or analyzed cases. However, no single nucleotide polymorphism was identified in exon 5 of GABRG2 in a Pakistani population, in contrast to a study of Chinese patients with childhood absence epilepsy.
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Authors
Muhammad Javed Iqbal, Muhammad Wasim, Umer Rashid, Nadia Zeeshan, Rizwan Ali, Sawera Nayyab, Sahrish Habib, Bushra Manzoor, Nouman Zahid,