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1 Ergebnisse
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Monoallelic and bi-allelic variants in NCDN cause neurodeve..:
Fatima, Ambrin
;
Hoeber, Jan
;
Schuster, Jens
...
The American Journal of Human Genetics. 109 (2022) 3 - p. 542-546 , 2022
Link:
https://doi.org/10.1016/j.ajhg.2022.02.007
RT Journal T1 <Title>Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ajhg.2022.02.007&Exemplar=1&LAN=DE A1 Fatima, Ambrin A1 Hoeber, Jan A1 Schuster, Jens A1 Koshimizu, Eriko A1 Maya-Gonzalez, Carolina A1 Keren, Boris A1 Mignot, Cyril A1 Akram, Talia A1 Ali, Zafar A1 Miyatake, Satoko A1 Tanigawa, Junpei A1 Koike, Takayoshi A1 Kato, Mitsuhiro A1 Murakami, Yoshiko A1 Abdullah, Uzma A1 Ali, Muhammad Akhtar A1 Fadoul, Rein A1 Laan, Loora A1 Castillejo-López, Casimiro A1 Liik, Maarika A1 Jin, Zhe A1 Birnir, Bryndis A1 Matsumoto, Naomichi A1 Baig, Shahid M. A1 Klar, Joakim A1 Dahl, Niklas PB Elsevier BV YR 2022 SN 0002-9297 JF The American Journal of Human Genetics VO 109 IS 3 SP 542 OP 546 LK http://dx.doi.org/https://doi.org/10.1016/j.ajhg.2022.02.007 DO https://doi.org/10.1016/j.ajhg.2022.02.007 SF ELIB - SuUB Bremen
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