Publications

学术论文（眼遗传+）

  • 1. CLEC3B Is A Novel Causative Gene for Macular-retinal Dystrophy.

    Zhou R, Mawatari G, Cai XB, Shen RJ, Wang YH, Wang YT, Guo YM, Guo FY, Yuan J, Pan D*, Nao-i N*, Jin ZB*.

    Genetics in Medicine. 2022 in press.

  • 2. Mutation of SLC7A14 Causes Auditory Neuropathy and Retinitis Pigmentosa Mediated by Lysosomal Dysfunction.

    Giffen KP, Li Y, Liu H, Zhao XC, Zhang CJ, Shen RJ, Wang T, Janesick A, Chen BP, Gong SS, Kachar B, Jin ZB*, He DZ*.

    Science Advances. 2022 in press.

  • 3. Fundus Tessellated Density of Pathologic Myopia.

    He HL#, Liu YX #, Chen XY, Ling SG, Qi Y, Xiong Y, Jin ZB*.

    Asia-Pacific Journal of Ophthalmology. 2023 in press.

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