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Whole-Genome Linkage Analysis with Whole-Exome Sequencing Identifies a Novel Frameshift Variant in NEFH in a Chinese Family with Charcot-Marie-Tooth 2: A Novel Variant in NEFH for Charcot-Marie-Tooth 2.
Bian X, Lin P, Li J, Long F, Duan R, Yuan Q, Li Y, Gao F, Gao S, Wei S, Li X, Sun W, Gong Y, Yan C, Liu Q. Bian X, et al. Among authors: wei s. Neurodegener Dis. 2018;18(2-3):74-83. doi: 10.1159/000487754. Epub 2018 Mar 27. Neurodegener Dis. 2018. PMID: 29587262
ORMDL3 and its implication in inflammatory disorders.
Ma X, Long F, Yun Y, Dang J, Wei S, Zhang Q, Li J, Zhang H, Zhang W, Wang Z, Liu Q, Zou C. Ma X, et al. Among authors: wei s. Int J Rheum Dis. 2018 Jun;21(6):1154-1162. doi: 10.1111/1756-185X.13324. Int J Rheum Dis. 2018. PMID: 29879314 Review.
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