Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly by Uctepe, Eyyup, Vona, Barbara, Esen, Fatma Nisa, Sonmez, F Mujgan, Smol, Thomas, Tümer, Sait, Mancılar, Hanifenur, Geylan Durgun, Dilan Ece, Boute, Odile, Moghbeli, Meysam, Ghayoor Karimiani, Ehsan, Hashemi, Narges, Bakhshoodeh, Behnoosh, Kim, Hyung Goo, Maroofian, Reza, Yesilyurt, Ahmet

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