与FAM111B相关的皮质皮质病和表型谱扩张中的乌比基蛋白酶系统失调:新病例报告和长期随访

Virginie Vignard1, Mike Maillasson2, Anne Bigot3

  • 1Nantes Université, CNRS, INSERM, l'institut du Thorax, Nantes 44000, France.

EBioMedicine
|August 21, 2025
PubMed
概括

由FAM111B突变引起的遗传性纤维化疾病POIKTMP,涉及到功能障碍的泛素蛋白酶系统 (UPS). 这一发现为POIKTMP患者提供了新的治疗点.

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