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Murine GRXCR1 Has a Different Function Than GRXCR2 in the Morphogenesis of Stereocilia
Mutations in human glutaredoxin domain-containing cysteine-rich protein 1 (GRXCR1) and its paralog GRXCR2 have been linked to hearing loss in humans. Although both GRXCR1 and GRXCR2 are required for the morphogenesis of stereocilia in cochlear hair cells, a fundamental question that remains unclear...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Frontiers Media S.A.
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8333275/ https://www.ncbi.nlm.nih.gov/pubmed/34366792 http://dx.doi.org/10.3389/fncel.2021.714070 |