CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow von Kim, Angelina Haesoo, Sakin, Irmak, Viviano, Stephen, Tuncel, Gulten, Aguilera, Stephanie Marie, Goles, Gizem, Jeffries, Lauren, Ji, Weizhen, Lakhani, Saquib A, Kose, Canan Ceylan, Silan, Fatma, Oner, Sukru Sadik, Kaplan, Oktay I, Ergoren, Mahmut Cerkez, Mishra-Gorur, Ketu, Gunel, Murat, Sag, Sebnem Ozemri, Temel, Sehime G, Deniz, Engin

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