A novel ZIC3 gene mutation identified in patients with heterotaxy and congenital heart disease

Heterotaxy syndrome (HTX) is characterized by left-right (LR) asymmetry disturbances associated with severe heart malformations. However, the exact genetic cause of HTX pathogenesis remains unclear. The aim of this study was to investigate the pathogenic mechanism underlying heterotaxy syndrome. Tar...

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I publikationen:Sci Rep
Huvudupphovsmän: Li, Shuolin, Liu, Sida, Chen, Weicheng, Yuan, Yuan, Gu, Ruoyi, Song, Yangliu, Li, Jian, Cao, Yinyin, Lin, Yixiang, Xu, Jun, Wang, Huijun, Ma, Duan, Ma, Xiaojing, Sheng, Wei, Huang, Guoying
Materialtyp: Artigo
Språk:Inglês
Publicerad: Nature Publishing Group UK 2018
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC6098004/
https://ncbi.nlm.nih.gov/pubmed/30120289
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-018-30204-3
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