Usher syndrome proteins ADGRV1 (USH2C) and CIB2 (USH1J) interact and share a common interactome containing TRiC/CCT-BBS chaperonins
The human Usher syndrome (USH) is the most common form of a sensory hereditary ciliopathy characterized by progressive vision and hearing loss. Mutations in the genes ADGRV1 and CIB2 have been associated with two distinct sub-types of USH, namely, USH2C and USH1J. The proteins encoded by the two gen...
Những tác giả chính: | , , , , , |
---|---|
Định dạng: | Bài viết |
Ngôn ngữ: | English |
Được phát hành: |
Frontiers Media S.A.
2023-06-01
|
Loạt: | Frontiers in Cell and Developmental Biology |
Những chủ đề: | |
Truy cập trực tuyến: | https://www.frontiersin.org/articles/10.3389/fcell.2023.1199069/full |