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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6098004/
https://www.ncbi.nlm.nih.gov/pubmed/30120289
http://dx.doi.org/10.1038/s41598-018-30204-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6098004/
https://www.ncbi.nlm.nih.gov/pubmed/30120289
http://dx.doi.org/10.1038/s41598-018-30204-3

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