Genotypic and Phenotypic Characteristics of 29 Patients With Rare Types of Osteogenesis Imperfecta: Average 5 Years of Follow-Up

Osteogenesis imperfecta (OI) is a rare genetic disorder characterized by bone fragility and abnormal connective tissue. Ninety percent of OI patients are caused by two mutations of COL1A1 and COL1A2, and more investigation was needed to better understand the rare types of OI. We followed up 29 patie...

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Váldodahkkit:	Lei Xi, Hao Zhang, Zhen-Lin Zhang
Materiálatiipa:	Artigo
Giella:	Inglês
Almmustuhtton:	Frontiers Media S.A. 2021-07-01
Ráidu:	Frontiers in Genetics
Fáttát:	osteogenesis imperfecta follow-up rare type bisphosphonates bone mineral density
Liŋkkat:	https://www.frontiersin.org/articles/10.3389/fgene.2021.622078/full
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