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Rare EIF4A2 variants are associated with a neurodevelopment..:
Paul, Maimuna S.
;
Duncan, Anna R.
;
Genetti, Casie A.
...
The American Journal of Human Genetics. 110 (2023) 1 - p. 120-145 , 2023
Link:
https://doi.org/10.1016/j.ajhg.2022.11.011
RT Journal T1
Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ajhg.2022.11.011&Exemplar=1&LAN=DE A1 Paul, Maimuna S. A1 Duncan, Anna R. A1 Genetti, Casie A. A1 Pan, Hongling A1 Jackson, Adam A1 Grant, Patricia E. A1 Shi, Jiahai A1 Pinelli, Michele A1 Brunetti-Pierri, Nicola A1 Garza-Flores, Alexandra A1 Shahani, Dave A1 Saneto, Russell P. A1 Zampino, Giuseppe A1 Leoni, Chiara A1 Agolini, Emanuele A1 Novelli, Antonio A1 Blümlein, Ulrike A1 Haack, Tobias B. A1 Heinritz, Wolfram A1 Matzker, Eva A1 Alhaddad, Bader A1 Abou Jamra, Rami A1 Bartolomaeus, Tobias A1 AlHamdan, Saber A1 Carapito, Raphael A1 Isidor, Bertrand A1 Bahram, Seiamak A1 Ritter, Alyssa A1 Izumi, Kosuke A1 Shakked, Ben Pode PB Elsevier BV YR 2023 SN 0002-9297 JF The American Journal of Human Genetics VO 110 IS 1 SP 120 OP 145 LK http://dx.doi.org/https://doi.org/10.1016/j.ajhg.2022.11.011 DO https://doi.org/10.1016/j.ajhg.2022.11.011 SF ELIB - SuUB Bremen
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