Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy
Ambrin Fatima(Uppsala University), Niklas Dahl(Uppsala University), Talia Akram(Uppsala University), Joakim Klar(University of Helsinki), Boris Keren(Sorbonne Université), Junpei Tanigawa(The University of Osaka), Muhammad Akhtar Ali(Quaid-i-Azam University), Satoko Miyatake(Yokohama City University Hospital), Zhe Jin(Uppsala University), Takayoshi Koike(National Epilepsy Center), Rein Fadoul(Uppsala University), Eriko Koshimizu(Yokohama City University), Carolina Maya‐González(Uppsala University), Casimiro Castillejo-López(Lund University), Mitsuhiro Kato(Showa University), Jens Schuster(Uppsala University), Bryndis Birnir(Uppsala University), Maarika Liik(Uppsala University Hospital), Shahid Mahmood Baig(National Institute for Biotechnology and Genetic Engineering), Uzma Abdullah(Pir Mehr Ali Shah Arid Agriculture University), Zafar Ali(University of Swat), Loora Laan(Uppsala University), Cyril Mignot(Sorbonne Université), Yoshiko Murakami(The University of Osaka), Naomichi Matsumoto(Yokohama City University), Jan Hoeber(Uppsala University)
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