A human stem cell resource to decipher the biochemical and cellular basis of neurodevelopmental defects in Lowe syndrome.

Biol Open · 2022 · PMC8822356 · PMID 35023542

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GO analysis of this gene set also revealed strong enrichment of GO terms suggesting altered neural development with the most highly significant GO terms being neurogenesis and nervous system development and function ( Fig. 6 E; Table S3 ).

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