Discovery and functional analysis of a new CRYBB1 deletion mutation linked to autosomal dominant congenital cataract in a Chinese family - Quiz - MDSpire
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Discovery and functional analysis of a new CRYBB1 deletion mutation linked to autosomal dominant congenital cataract in a Chinese family

  • By

  • Li Li

  • Jianfei Yue

  • Jiaxi Song

  • Meiling Qin

  • Shuyu Zhou

  • Jingfan Liu

  • Guangying Zheng

  • January 20, 2026

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Original Source(s)

Discovery and functional analysis of a new CRYBB1 deletion mutation linked to autosomal dominant congenital cataract in a Chinese family

  • by Li Li, Jianfei Yue, Jiaxi Song, Meiling Qin, Shuyu Zhou, Jingfan Liu, Guangying Zheng

  • January 20, 2026

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