A Frameshift Mutation Results in a Truncated Nonfunctional Carboxyl-terminal Proα1(I) Propeptide of Type I Collagen in Osteogenesis Imperfecta
Open Access
- 1 July 1989
- journal article
- Published by Elsevier
- Vol. 264 (19) , 10960-10964
- https://doi.org/10.1016/s0021-9258(18)60412-0
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Perinatal lethal osteogenesis imperfecta in transgenic mice bearing an engineered mutant pro-α1(I) collagen geneNature, 1988
- Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA PolymeraseScience, 1988
- Subtle structural alterations in the chains of type I procollagen produce osteogenesis imperfecta type IINature, 1985
- Heritable Diseases of CollagenNew England Journal of Medicine, 1984
- Human proα1(I) collagen gene structure reveals evolutionary conservation of a pattern of introns and exonsNature, 1984
- Nucleotide sequences of complementary deoxyribonucleic acids for the pro.alpha.1 chain of human type I procollagen. Statistical evaluation of structures that are conserved during evolutionBiochemistry, 1983
- Internal deletion in a collagen gene in a perinatal lethal form of osteogenesis imperfectaNature, 1983
- Kinetics of reduction of the intersubunit disulfides of the carboxyl propeptide of type I procollagenBiochemistry, 1982
- Primary structure of the carbohydrate‐containing regions of the carboxyl propeptides of type I procollagenFEBS Letters, 1981
- Use of a mixture of proteinase-free collagenases for the specific assay of radioactive collagen in the presence of other proteinsBiochemistry, 1971