Centriole structural integrity defects are a crucial feature of Hydrolethalus Syndrome
A. Curinha, Z. Huang, T. Anglen, M. A. Strong, C. R. Gliech, C. E. Jewett, A. Friskes, A. J. Holland
This study shows that HYLS1 mutations cause centriole structural defects leading to ciliary dysfunction and developmental issues in mice, mirroring human Hydrolethalus Syndrome.
bioRxiv · Mar 6, 2024Cell Biology