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Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy |
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Titel: |
Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy |
Auteur: |
Fatima, Ambrin Hoeber, Jan Schuster, Jens Koshimizu, Eriko Maya-Gonzalez, Carolina Keren, Boris Mignot, Cyril Akram, Talia Ali, Zafar Miyatake, Satoko Tanigawa, Junpei Koike, Takayoshi Kato, Mitsuhiro Murakami, Yoshiko Abdullah, Uzma Ali, Muhammad Akhtar Fadoul, Rein Laan, Loora Castillejo-López, Casimiro Liik, Maarika Jin, Zhe Birnir, Bryndis Matsumoto, Naomichi Baig, Shahid M. Klar, Joakim Dahl, Niklas |
Verschenen in: |
The American journal of human genetics |
Paginering: |
Jaargang 108 () nr. 4 pagina's 739-748 |
Jaar: |
2021 |
Inhoud: |
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Uitgever: |
The Authors |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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