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  1. Article

    Open Access

    A novel mutation in the PRPH2 gene in a Chinese pedigree with retinitis pigmentosa and angle-closure glaucoma

    Retinitis pigmentosa (RP) is a rare, progressive, and hereditary disorder that leads to the progressive loss of vision and visual field, and in some cases blindness. The specific relationship between RP and gl...

    Wei-ning Li, **u-juan Du, Yu-ting Zhang, Le-yi Wang, **g Zhu in BMC Ophthalmology (2021)

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