Structure and Membrane Targeting of the PDZD7 Harmonin Homology Domain (HHD) Associated With Hearing Loss

Usher syndrome (USH) is the leading cause of hereditary hearing–vision loss in humans. PDZ domain-containing 7 (PDZD7) has been reported to be a modifier of and contributor to USH. PDZD7 co-localizes with USH2 proteins in the inner ear hair cells and is essential for ankle-link formation and stereoc...

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Detalles Bibliográficos
Autores principales: Lin, Lin, Wang, Huang, Ren, Decheng, Xia, Yitian, He, Guang, Lu, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8083959/
https://www.ncbi.nlm.nih.gov/pubmed/33937240
http://dx.doi.org/10.3389/fcell.2021.642666

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8083959/
https://www.ncbi.nlm.nih.gov/pubmed/33937240
http://dx.doi.org/10.3389/fcell.2021.642666

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