A novel cryptic splice site mutation in COL1A2 as a cause of osteogenesis imperfecta

Osteogenesis imperfecta (OI) is an inherited genetic disorder characterized by frequent bone fractures and reduced bone mass. Most cases of OI are caused by dominantly inherited heterozygous mutations in one of the two genes encoding type I collagen, COL1A1 and COL1A2. Here we describe a five-year-o...

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Detalles Bibliográficos
Autores principales: El-Gazzar, Ahmed, Mayr, Johannes A., Voraberger, Barbara, Brugger, Karin, Blouin, Stéphane, Tischlinger, Katharina, Duba, Hans-Christoph, Prokisch, Holger, Fratzl-Zelman, Nadja, Högler, Wolfgang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8339231/
https://www.ncbi.nlm.nih.gov/pubmed/34381850
http://dx.doi.org/10.1016/j.bonr.2021.101110

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8339231/
https://www.ncbi.nlm.nih.gov/pubmed/34381850
http://dx.doi.org/10.1016/j.bonr.2021.101110

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