SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients

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 unknown CHD genes within these intervals. Here, we have shown that knockdown of SORBS2...

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Detalles Bibliográficos
Autores principales: Liang, Fei, Wang, Bo, Geng, Juan, You, Guoling, Fa, Jingjing, Zhang, Min, Sun, Hunying, Chen, Huiwen, Fu, Qihua, Zhang, Xiaoqing, Zhang, Zhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186900/
https://www.ncbi.nlm.nih.gov/pubmed/34099102
http://dx.doi.org/10.7554/eLife.67481

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186900/
https://www.ncbi.nlm.nih.gov/pubmed/34099102
http://dx.doi.org/10.7554/eLife.67481

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