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....

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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

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