Liang Jin

Bioinformatic analysis of the role of solute carrier-glutamine transporters in breast cancer

Yujie Liu, Xin Zhao, Zhenzhen Liu, 2022, Annals of translational medicine.

Genotype and clinical course in 2 Chinese Han siblings with Wilson disease presenting with isolated disabling premature osteoarthritis

T. Dai, Lili Cao, Bingquan Leng, 2017, Medicine.

Expanding the phenotypic spectrum of KCNK4: From syndromic neurodevelopmental disorder to rolandic epilepsy

Jing Zhou, Qiang Guo, Sheng Luo, 2023, Frontiers in Molecular Neuroscience.

Clinical and genetic analysis of Christianson syndrome caused by variant of SLC9A6: case report and literature review

Mengchun Li, Lijun Wang, T. Jia, 2023, Frontiers in Neurology.

SZT2 variants associated with partial epilepsy or epileptic encephalopathy and the genotype-phenotype correlation

Y. Chen, Zhigang Liu, L. Gao, 2023, Frontiers in Molecular Neuroscience.

Recessive APC2 missense variants associated with epilepsies without neurodevelopmental disorders

Yun Li, N. He, Jianhang Guo, 2023, Seizure: European Journal of Epilepsy.