Phenotypic Properties of Collagen in Dentinogenesis Imperfecta Associated with Osteogenesis Imperfecta

INTRODUCTION: Dentinogenesis imperfecta type 1 (OIDI) is considered a relatively rare genetic disorder (1:5000 to 1:45,000) associated with osteogenesis imperfecta. OIDI impacts the formation of collagen fibrils in dentin, leading to morphological and structural changes that affect the strength and...

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Detalles Bibliográficos
Autores principales: Ibrahim, Salwa, Strange, Adam P, Aguayo, Sebastian, Shinawi, Albatool, Harith, Nabilah, Mohamed-Ibrahim, Nurjehan, Siddiqui, Samera, Parekh, Susan, Bozec, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6897053/
https://www.ncbi.nlm.nih.gov/pubmed/31819441
http://dx.doi.org/10.2147/IJN.S217420

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6897053/
https://www.ncbi.nlm.nih.gov/pubmed/31819441
http://dx.doi.org/10.2147/IJN.S217420

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