Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease

Congenital heart disease (CHD) is the most frequent kind of birth deformity in human beings and the leading cause of neonatal mortality worldwide. Although genetic etiologies encompassing aneuploidy, copy number variations, and mutations in over 100 genes have been uncovered to be involved in the pa...

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Detalles Bibliográficos
Autores principales: Shi, Hong-Yu, Xie, Meng-Shi, Yang, Chen-Xi, Huang, Ri-Tai, Xue, Song, Liu, Xing-Yuan, Xu, Ying-Jia, Yang, Yi-Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406965/
https://www.ncbi.nlm.nih.gov/pubmed/36010266
http://dx.doi.org/10.3390/diagnostics12081917

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406965/
https://www.ncbi.nlm.nih.gov/pubmed/36010266
http://dx.doi.org/10.3390/diagnostics12081917

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