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Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis.
Zhang W, Li Y, Xu A, Ouyang Q, Wu L, Zhou D, Wu L, Zhang B, Zhao X, Wang Y, Wang X, Duan W, Wang Q, You H, Huang J, Ou X, Jia J; China Registry of Genetic/Metabolic Liver Diseases (CR-GMLD) Group. Zhang W, et al. Among authors: wu l. Orphanet J Rare Dis. 2022 Jun 6;17(1):216. doi: 10.1186/s13023-022-02349-y. Orphanet J Rare Dis. 2022. PMID: 35668470 Free PMC article.
Human iPSC-derived microglia sense and dampen hyperexcitability of cortical neurons carrying the epilepsy-associated SCN2A-L1342P mutation.
Que Z, Olivero-Acosta MI, Robinson M, Chen I, Zhang J, Wettschurack K, Wu J, Xiao T, Otterbacher CM, Shankar V, Harlow H, Hong S, Zirkle B, Wang M, Cui N, Mandal P, Chen X, Deming B, Halurkar M, Zhao Y, Rochet JC, Xu R, Brewster AL, Wu LJ, Yuan C, Skarnes WC, Yang Y. Que Z, et al. Among authors: wu lj. J Neurosci. 2024 Nov 18:e2027232024. doi: 10.1523/JNEUROSCI.2027-23.2024. Online ahead of print. J Neurosci. 2024. PMID: 39557580
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