Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy
Ambrin Fatima(Aga Khan 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(Shiga University of Medical Science), Rein Fadoul(Uppsala University), Eriko Koshimizu(Yokohama City University), Carolina Maya‐González(Karolinska Institutet), Casimiro Castillejo-López(Lund University), Mitsuhiro Kato(Showa University), Takayoshi Koike(Hokkaido 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), Loora Laan(Uppsala University), Cyril Mignot(Sorbonne Université), Naomichi Matsumoto(Yokohama City University), Yoshiko Murakami(Hidaka Hospital), Zhe Jin, Jan Hoeber(Uppsala University)
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