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A novel KCNQ2 gene mutation in a patient with self-limitted non-familial neonatal epilepsy: a case report
TRUNG HIEU LE NGUYEN, QUYNH MAI THI NGUYEN, KHANH VAN THI LE, MINH THU THUY LE, ANH NGAN TRAN LE, HUY PHUOC DO, HIEN THI DIEU HUYNH, THU HANG THI DO
94-101
2021-02-21
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An optimized method for detection of MECP2 point mutations in Vietnamese children with rett syndrome
VÂN THỊ KHÁNH LÊ, DƯƠNG DUY THÁI LÊ, HẰNG THỊ THU ĐỖ, KIỀU THỊ THÚY HUỲNH, HIẾU TRUNG NGUYỄN LÊ, DUNG THỊ THÙY BÙI, VŨ THANH NGUYỄN, DŨNG QUỐC NGUYỄN, HIEN THI DIEU HUYNH
27-34
2020-11-10
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