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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Int J Nanomedicine
Päätekijät: Ibrahim, Salwa, Strange, Adam P, Aguayo, Sebastian, Shinawi, Albatool, Harith, Nabilah, Mohamed-Ibrahim, Nurjehan, Siddiqui, Samera, Parekh, Susan, Bozec, Laurent
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Dove 2019
Aiheet:
Original Research
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6897053/
https://ncbi.nlm.nih.gov/pubmed/31819441
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/IJN.S217420
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