Exploration of the skeletal phenotype of the Col1a1 (+/Mov13) mouse model for haploinsufficient osteogenesis imperfecta type 1

INTRODUCTION: Osteogenesis Imperfecta is a rare genetic connective tissue disorder, characterized by skeletal dysplasia and fragile bones. Currently only two mouse models have been reported for haploinsufficient (HI) mild Osteogenesis Imperfecta (OI); the Col1a1 (+/Mov13) (Mov13) and the Col1a1 (+/-...

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Detalles Bibliográficos
Autores principales: Claeys, Lauria, Zhytnik, Lidiia, Wisse, Lisanne E., van Essen, Huib W., Eekhoff, E. Marelise W., Pals, Gerard, Bravenboer, Nathalie, Micha, Dimitra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031054/
https://www.ncbi.nlm.nih.gov/pubmed/36967771
http://dx.doi.org/10.3389/fendo.2023.1145125

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031054/
https://www.ncbi.nlm.nih.gov/pubmed/36967771
http://dx.doi.org/10.3389/fendo.2023.1145125

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