RTTN

Publications

Shamseldin H, et al. RTTN mutations cause primary microcephaly and primordial dwarfism in humans. Am J Hum Genet. 2015;97(6):862-868. PMID: 26608784.

Kheradmand Kia S, et al. RTTN mutations link primary cilia function to organization of the human cerebral cortex. Am J Hum Genet. 2012;91(3):533-540.