Wanqi Wang

A nonsense mutation in the CUL3 gene in a Chinese patient with autism spectrum disorder and epilepsy: A case report

Qiandui Chen, Jiayi Li, Shuangzhu Lin, 2022, Medicine.

Thyroid hormone resistance resulting from a novel mutation in the THRB gene in a Chinese child: A case report

J. Feng, Wen Wang, Qiandui Chen, 2023, Medicine.

Developmental and epileptic encephalopathy 44 due to compound heterozygous variants in the UBA5 gene: a case report

Qi-jun Pang, Cui Wang, Shuangzhu Lin, 2023, Acta Epileptologica.

A case of Sandhoff disease caused by a novel β-hexosaminidase B (HEXB) mutation c.118delG (p.A40fs*24): A case report from China

Yang Chen, Xiaochun Feng, Qiandui Chen, 2023, Medicine.