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CRISPR single base editing, neuronal disease modelling and functional genomics for genetic variant analysis: pipeline validation using Kleefstra syndrome EHMT1 haploinsufficiency

Title:	CRISPR single base editing, neuronal disease modelling and functional genomics for genetic variant analysis: pipeline validation using Kleefstra syndrome EHMT1 haploinsufficiency
Authors:	Fear, Vanessa S.^{Aff1, IDs13287022027403_cor1}; Forbes, Catherine A.^Aff1; Anderson, Denise^Aff2; Rauschert, Sebastian^Aff2; Syn, Genevieve^Aff2; Shaw, Nicole^Aff1; Jamieson, Sarra^Aff2; Ward, Michelle^Aff4; Baynam, Gareth^{Aff3, Aff4}; Lassmann, Timo^{Aff1, Aff2}
Source:	Stem Cell Research & Therapy. 13(1)
Database:	Springer Nature Journals