Fangrui Wu

Early diagnosis improving the outcome of an infant with epileptic encephalopathy with cytoplasmic FMRP interacting protein 2 mutation

Li Jiang, Si-qi Hong, S. Liao, 2019, Medicine.

Novel VAC14 variants identified in two Chinese siblings with childhood‐onset striatonigral degeneration

S. Liao, Min Zhong, Ying Dai, 2019, Molecular genetics & genomic medicine.

Early-onset epilepsy and microcephaly-capillary malformation syndrome caused by a novel STAMBP mutation in a Chinese boy

Li Jiang, Juan Wang, S. Liao, 2019, Molecular Medicine Reports.