MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathwayMaolei Gong, Dominique Braun, Haoran Liu et al.|The American Journal of Human Genetics|2024Cited by 19
Novel RRAGD Variants in Autosomal Dominant Kidney Hypomagnesemia and Therapeutic PerspectivesAnastasia Adella, Jeroen H. F. de Baaij, François Jouret et al.|Kidney International Reports|2025Cited by 4
<i>MARK2</i> variants cause autism spectrum disorder <i>via</i> the downregulation of WNT/β-catenin signaling pathwayMaolei Gong, Scott McLean, Jiayi Li et al.|medRxiv|2024Cited by 0