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"Haemochromatotic" characteristics of the human BEL-7402 cell line.
Xu A, Li Y, Chen W, Li X, Zhang W, Li S, Wu L, Wu Z, Zhang B, Ou X, Huang J. Xu A, et al. Among authors: wu l, wu z. Br J Haematol. 2018 Oct;183(2):302-306. doi: 10.1111/bjh.14952. Epub 2017 Sep 29. Br J Haematol. 2018. PMID: 28961311 Free article. No abstract available.
A novel SLC40A1 p.Y333H mutation with gain of function of ferroportin: A recurrent cause of haemochromatosis in China.
Zhang W, Xu A, Li Y, Zhao S, Zhou D, Wu L, Zhang B, Zhao X, Wang Y, Wang X, Duan W, Wang Q, Nan Y, You H, Jia J, Ou X, Huang J; China Registry of Genetic/Metabolic Liver Diseases (CR-GMLD) Group. Zhang W, et al. Among authors: wu l. Liver Int. 2019 Jun;39(6):1120-1127. doi: 10.1111/liv.14013. Epub 2018 Dec 28. Liver Int. 2019. PMID: 30500107
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.
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