Fei Shen

De Novo CSNK2B Mutations in Five Cases of Poirier–Bienvenu Neurodevelopmental Syndrome

Z. Qin, Shan Ou, Qinle Zhang, 2022, Frontiers in Neurology.

Case Report: Variations in the ALPL Gene in Chinese Patients With Hypophosphatasia

Z. Qin, Qiang Zhang, Shang Yi, 2021, Frontiers in Genetics.

Novel compound heterozygous variant of BSCL2 identified by whole exome sequencing and multiplex ligation-dependent probe amplification in an infant with congenital generalized lipodystrophy

Yiping Shen, Z. Qin, Shang Yi, 2020, Molecular medicine reports.

Targeted addition of mini-dystrophin into rDNA locus of Duchenne muscular dystrophy patient-derived iPSCs.

D. Liang, Lingqian Wu, Zhiqing Hu, 2021, Biochemical and biophysical research communications.

PREPL Deficiency: A Homozygous Splice Site PREPL Mutation in a Patient With Congenital Myasthenic Syndrome and Absence of Ovaries and Hypoplasia of Uterus

Mengting Li, Qiang Zhang, Shang Yi, 2020, Frontiers in Genetics.