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Three Patient Kindred with a Novel Phenotype of Osteogenesis Imperfecta due to a COL1A1 Variant

Osteogenesis imperfecta (OI) is characterized by fractures and progressive bone deformities. Fracture rates peak during the toddler and adolescent years and decline during adulthood but do not stop entirely. We describe a kindred, the affected members of which were the mother and two sons, who prese...

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Detalles Bibliográficos
Autores principales:	Gupta, Nidhi, Gregory, Seth W., Deyle, David R., Tebben, Peter J.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Galenos Publishing 2021
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186326/ https://www.ncbi.nlm.nih.gov/pubmed/32519829 http://dx.doi.org/10.4274/jcrpe.galenos.2020.2020.0012

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