Characterization of human bone morphogenetic protein gene variants for possible roles in congenital heart disease

Congenital heart disease (CHD) is a complex illness with high rates of morbidity and mortality. In embryonic development, the heart is the first formed organ, which is strictly controlled by gene regulatory networks, including transcription factors, signaling pathways, epigenetic factors and microRN...

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Detalles Bibliográficos
Autores principales: Li, Fei Feng, Deng, Xia, Zhou, Jing, Yan, Peng, Zhao, Er Ying, Liu, Shu Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4940093/
https://www.ncbi.nlm.nih.gov/pubmed/27357418
http://dx.doi.org/10.3892/mmr.2016.5428

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4940093/
https://www.ncbi.nlm.nih.gov/pubmed/27357418
http://dx.doi.org/10.3892/mmr.2016.5428

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