Whole exome sequencing identified a novel missense mutation in EPM2A underlying Lafora disease in a Pakistani family

Whole exome sequencing identified a novel missense mutation in EPM2A underlying Lafora disease in a Pakistani family

Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Seizure - Volume 51, October 2017, Pages 200-203

Zain Aslam, Eungi Lee, Mazhar Badshah, Muhammad Naeem, Changsoo Kang,