Xiao-ying Wang

发表

Mutation analysis of CACNA1S and SCN4A in patients with hypokalemic periodic paralysis.

Xiao-ying Wang, Bing-Wen Ren, Zeng-Hua Yong, 2015, Molecular medicine reports.

Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome.

Zhaoxia Wang, Yun Yuan, Y. Qi, 2006, Chinese medical journal.

Phospholemman, a major regulator of skeletal muscle Na+/K+-ATPase, is not mutated in probands with hypokalemic periodic paralysis.

Ying-ying Chen, Xiao-ying Wang, Qiuxia Fu, 2017, Experimental and therapeutic medicine.