Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy
Am J Hum Genet
.
2022 Mar 3;109(3):542-546.
doi: 10.1016/j.ajhg.2022.02.007.
Authors
Ambrin Fatima
,
Jan Hoeber
,
Jens Schuster
,
Eriko Koshimizu
,
Carolina Maya-Gonzalez
,
Boris Keren
,
Cyril Mignot
,
Talia Akram
,
Zafar Ali
,
Satoko Miyatake
,
Junpei Tanigawa
,
Takayoshi Koike
,
Mitsuhiro Kato
,
Yoshiko Murakami
,
Uzma Abdullah
,
Muhammad Akhtar Ali
,
Rein Fadoul
,
Loora Laan
,
Casimiro Castillejo-López
,
Maarika Liik
,
Zhe Jin
,
Bryndis Birnir
,
Naomichi Matsumoto
,
Shahid M Baig
,
Joakim Klar
,
Niklas Dahl
PMID:
35245475
PMCID:
PMC8948155
DOI:
10.1016/j.ajhg.2022.02.007
No abstract available
Publication types
Published Erratum