Xianglian Tang

Compound heterozygous WDR19 variants associated with nephronophthisis, Caroli disease, refractory epilepsy and congenital bilateral central blindness: Case report

Shang Yi, Qi Yang, Sheng Yi, 2023, Heliyon.

A nonsense CC2D1A variant is associated with congenital anomalies, motor delay, hypotonia, and slight deformities

Shang Yi, Sheng Yi, Limei Huang, 2024, Heliyon.