Three de novo variants in KMT2A (MLL) identified by whole exome sequencing in patients with Wiedemann-Steiner syndrome.
Sukun LuoBo BiWenqian ZhangRui ZhouWei ChenPeiwei ZhaoYufeng HuangLi YuanXuelian HePublished in: Molecular genetics & genomic medicine (2021)
Our study would aid in further broadening our knowledge about the genotype-phenotype correlation of WSS.
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