Transgenic mouse model of the mild dominant form of osteogenesis imperfecta.

Osteogenesis imperfecta type I is a mild, dominantly inherited, connective tissue disorder characterized by bone fragility. Mutations in type I collagen account for all known cases. In Mov-13 mice, integration of a murine retrovirus within the first intron of the alpha 1(I) collagen gene results in...

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Bibliografiska uppgifter
Huvudupphovsmän: Bonadio, J, Saunders, T L, Tsai, E, Goldstein, S A, Morris-Wiman, J, Brinkley, L, Dolan, D F, Altschuler, R A, Hawkins, J E, Bateman, J F
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1990
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC54700/
https://ncbi.nlm.nih.gov/pubmed/2402497
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