Cardiovascular abnormalities and its correlation with genotypes of children with osteogenesis imperfecta

BACKGROUND AND OBJECTIVES: Osteogenesis imperfecta (OI) is a rare disorder of abnormal production or modification of type I collagen, which is caused by mutations in COL1A1, COL1A2 or other genes. We investigate the cardiac abnormalities and its correlation with pathogenic mutations in OI children....

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Dichen, Liu, Yongtai, Liu, Jidong, Hu, Jing, Zhang, Qian, Wang, Ou, Jiang, Yan, Xia, Weibo, Xing, Xiaoping, Li, Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9632612/
https://www.ncbi.nlm.nih.gov/pubmed/36339400
http://dx.doi.org/10.3389/fendo.2022.1004946

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9632612/
https://www.ncbi.nlm.nih.gov/pubmed/36339400
http://dx.doi.org/10.3389/fendo.2022.1004946

Ejemplares similares