.

Fabrizio Vacca1, Binnaz Yalcin2, Muhammad Ansar1,3

  • 1Department of Ophthalmology, University of Lausanne, Jules Gonin Eye Hospital, Fondation Asile Des Aveugles, Lausanne, Switzerland.

PubMed
概括

科恩综合征 (CS) 是一种罕见的遗传疾病,与VPS13B基因突变有关. 这篇评论探讨了VPS13B蛋白功能,其细胞作用,以及这些与CS症状和动物模型的关系.

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