Tibial plateau fracture and RNA sequencing with osteogenesis imperfecta: a case report

Osteogenesis imperfecta (OI) is a hereditary skeletal dysplasia with an incidence of approximately 1:15,000 to 20,000. OI is usually caused by the mutation of COL1A1 and COL1A2, which would encode the α-chain of type I collagen. OI is clinically characterized by decreased bone mass, increased risk o...

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Detalles Bibliográficos
Autores principales: Chen, Yixiao, Li, Guoqing, Wei, Liangchen, Weng, Jian, Liu, Su, Gu, Mingxi, Liu, Pei, Zhu, Yuanchao, Xiong, Ao, Zeng, Hui, Yu, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203611/
https://www.ncbi.nlm.nih.gov/pubmed/37229455
http://dx.doi.org/10.3389/fendo.2023.1164386

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203611/
https://www.ncbi.nlm.nih.gov/pubmed/37229455
http://dx.doi.org/10.3389/fendo.2023.1164386

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