CRISPR single base editing, neuronal disease modelling and functional genomics for genetic variant analysis: pipeline validation using Kleefstra syndrome EHMT1 haploinsufficiency.
Vanessa S FearCatherine A ForbesDenise AndersonSebastian RauschertGenevieve SynNicole ShawSarra JamiesonMichelle WardGareth BaynamTimo LassmannPublished in: Stem cell research & therapy (2022)
The study pipeline is a rapid, robust method for genetic variant assessment that will support rare diseases patient diagnosis. The results also provide valuable information on genome wide perturbations key to disease mechanism that can be targeted for drug treatments.