DNAH11 variants and its association with congenital heart disease and heterotaxy syndrome

Congenital heart diseases (CHDs) are the most common types of birth defects, affecting approximately 1% of live births and remaining the leading cause of mortality. CHD patients often show a higher incidence of heterotaxy syndrome. However, the exact aetiology of CHD and heterotaxy syndrome remains...

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Detalles Bibliográficos
Autores principales: Liu, Sida, Chen, Weicheng, Zhan, Yongkun, Li, Shuolin, Ma, Xiaojing, Ma, Duan, Sheng, Wei, Huang, Guoying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491566/
https://www.ncbi.nlm.nih.gov/pubmed/31040315
http://dx.doi.org/10.1038/s41598-019-43109-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491566/
https://www.ncbi.nlm.nih.gov/pubmed/31040315
http://dx.doi.org/10.1038/s41598-019-43109-6

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