Three de novo variants in KMT2A (MLL) identified by whole exome sequencing in patients with Wiedemann –Steiner syndrome

ConclusionOur study would aid in further broadening our knowledge about the genotype –phenotype correlation of WSS.

Source: Molecular Genetics & Genomic Medicine - September 2, 2021 Category: Genetics & Stem Cells Authors: Sukun Luo, Bo Bi, Wenqian Zhang, Rui Zhou, Wei Chen, Peiwei Zhao, Yufeng Huang, Li Yuan, Xuelian He Tags: ORIGINAL ARTICLE Source Type: research