SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients
Elife. 2021 Jun 8;10:e67481. doi: 10.7554/eLife.67481. Fei Liang # 1 2, Bo Wang # 3, Juan Geng 3, Guoling You 3, Jingjing Fa 3, Min Zhang 2, Hunying Sun 4, Huiwen Chen 5, Qihua Fu 3, Xiaoqing Zhang 3, Zhen Zhang 2 PMID: 34099102 원본링크: https://pubmed.ncbi.nlm.nih.gov/34099102/ PMCID: PMC8186900 DOI: 10.7554/eLife.67481 Abstract Chromosome 4q deletion is one of the most frequently detected genomic imbalance events in congenital heart disease (CHD) patients. However, a portion of CHD-associated 4q deletions without known CHD genes suggests …