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Loss-of-function variants in SRRM2 cause a neurodevelopment..:
Cuinat, Silvestre
;
Nizon, Mathilde
;
Isidor, Bertrand
...
Genetics in Medicine. 24 (2022) 8 - p. 1774-1780 , 2022
Link:
https://doi.org/10.1016/j.gim.2022.04.011
RT Journal T1
Loss-of-function variants in SRRM2 cause a neurodevelopmental disorder
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.gim.2022.04.011&Exemplar=1&LAN=DE A1 Cuinat, Silvestre A1 Nizon, Mathilde A1 Isidor, Bertrand A1 Stegmann, Alexander A1 van Jaarsveld, Richard H. A1 van Gassen, Koen L. A1 van der Smagt, Jasper J. A1 Volker-Touw, Catharina M.L. A1 Holwerda, Sjoerd J.B. A1 Terhal, Paulien A. A1 Schuhmann, Sarah A1 Vasileiou, Georgia A1 Khalifa, Mohamed A1 Nugud, Alaa A. A1 Yasaei, Hemad A1 Ousager, Lilian Bomme A1 Brasch-Andersen, Charlotte A1 Deb, Wallid A1 Besnard, Thomas A1 Simon, Marleen E.H. A1 Amsterdam, Karin Huijsdens-van A1 Verbeek, Nienke E. A1 Matalon, Dena A1 Dykzeul, Natalie A1 White, Shana A1 Spiteri, Elizabeth A1 Devriendt, Koen A1 Boogaerts, Anneleen A1 Willemsen, Marjolein A1 Brunner, Han G. PB Elsevier BV YR 2022 SN 1098-3600 JF Genetics in Medicine VO 24 IS 8 SP 1774 OP 1780 LK http://dx.doi.org/https://doi.org/10.1016/j.gim.2022.04.011 DO https://doi.org/10.1016/j.gim.2022.04.011 SF ELIB - SuUB Bremen
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