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Multiple Sclerosis (Houndmills, Basingstoke, England)|July 10, 2018
Primary optic neuropathy in Behçet's syndromeQinglin Yang, Lin Sun, Qian Wang, et al.
Molecular Vision|January 16, 2014
Maternal germline mosaicism of kinesin family member 21A (KIF21A) mutation causes complex phenotypes in a Chinese family with congenital fibrosis of the extraocular musclesGang Liu, Xue Chen, Xiantao Sun, et al.
Orphanet Journal of Rare Diseases|December 10, 2022
Clinical and genetic characteristics of Chinese patients with congenital cranial dysinnervation disordersHongyan Jia, Qian Ma, Yi Liang, et al.
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