Filippi syndrome-associated CKAP2L modulates microtubule dynamics essential for mitosis and ciliary length regulation
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Mutations in the gene encoding cytoskeleton-associated protein 2-like (CKAP2L) have been identified as a causative factor for Filippi syndrome, a rare developmental disorder characterized by facial dysmorphism, syndactyly, and microcephaly. However, the cellul... ...
