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A novel MIP mutation in a Chinese family with congenital cataract.
Yuan C, Han T, Su P, Liu M, Zhou X, Zhang D, Jia W, Wang A, Yue M, Xiang Z, Chen L, Zhang X. Yuan C, et al. Among authors: zhang d, zhang x. Ophthalmic Genet. 2018 Aug;39(4):473-476. doi: 10.1080/13816810.2018.1484930. Ophthalmic Genet. 2018. PMID: 29947569
Two novel STAT1 mutations cause Mendelian susceptibility to mycobacterial disease.
Liu Z, Zhou M, Yuan C, Ni Z, Liu W, Tan Y, Zhang D, Zhou X, Zou T, Wang J, Hou M, Peng X, Zhang X. Liu Z, et al. Among authors: zhang d, zhang x. Biochem Biophys Res Commun. 2022 Feb 5;591:124-129. doi: 10.1016/j.bbrc.2021.11.036. Epub 2021 Nov 14. Biochem Biophys Res Commun. 2022. PMID: 34815077
Novel mutations in ZP2 and ZP3 cause female infertility in three patients.
Jia W, Xi Q, Zhu L, Luo Y, Li Z, Hou M, Zhang D, Yang X, Hu J, Jin L, Zhang X. Jia W, et al. Among authors: zhang d, zhang x. J Assist Reprod Genet. 2022 May;39(5):1205-1215. doi: 10.1007/s10815-022-02466-4. Epub 2022 Apr 3. J Assist Reprod Genet. 2022. PMID: 35366744 Free PMC article.
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