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A synonymous UPF3B variant causing a speech disorder implic..:
Domingo, Deepti
;
Nawaz, Urwah
;
Corbett, Mark
...
Human Molecular Genetics. 29 (2020) 15 - p. 2568-2578 , 2020
Link:
https://doi.org/10.1093/hmg/ddaa151
RT Journal T1
A synonymous UPF3B variant causing a speech disorder implicates NMD as a regulator of neurodevelopmental disorder gene networks
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_hmg_ddaa151&Exemplar=1&LAN=DE A1 Domingo, Deepti A1 Nawaz, Urwah A1 Corbett, Mark A1 Espinoza, Josh L A1 Tatton-Brown, Katrina A1 Coman, David A1 Wilkinson, Miles F A1 Gecz, Jozef A1 Jolly, Lachlan A PB Oxford University Press (OUP) YR 2020 SN 0964-6906 SN 1460-2083 JF Human Molecular Genetics VO 29 IS 15 SP 2568 OP 2578 LK http://dx.doi.org/https://doi.org/10.1093/hmg/ddaa151 DO https://doi.org/10.1093/hmg/ddaa151 SF ELIB - SuUB Bremen
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