A rare congenital anemia is caused by mutations in the centralspindlin complex
Sandeep N. Wontakal, Mishan Britto, Sarah Tannenbaum, Benjamin Heath Durham, Margaret T. Lee, Masanori Mishima
This study identifies compound heterozygous RACGAP1 variants causing CDAIII by disrupting the centralspindlin complex, leading to cytokinesis defects.
medRxiv · Apr 7, 2021 · PreprintGenetic & Genomic Medicine