RNA sequence analysis of a perinatal lethal osteogenesis imperfecta mutation
Open Access
- 1 June 1989
- journal article
- research article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 264 (17) , 10083-10087
- https://doi.org/10.1016/s0021-9258(18)81769-0
Abstract
No abstract availableThis publication has 26 references indexed in Scilit:
- Complete nucleotide sequence of the region encompassing the first twenty-five exons of the human proα 1(I) collagen gene (COL1A1)Gene, 1988
- Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations.Proceedings of the National Academy of Sciences, 1988
- Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA PolymeraseScience, 1988
- Genetics cracks bone diseaseNature, 1987
- Disease Diagnosis by Recombinant DNA MethodsScience, 1987
- Lethal osteogenesis imperfecta resulting from a single nucleotide change in one human pro alpha 1(I) collagen allele.Proceedings of the National Academy of Sciences, 1986
- Mitotic recombination in germ cells generated two major histocompatibility complex mutant genes shown to be identical by RNA sequence analysis: Kbm9 and Kbm6.Proceedings of the National Academy of Sciences, 1986
- Subtle structural alterations in the chains of type I procollagen produce osteogenesis imperfecta type IINature, 1985
- Nuclease S1 mapping of a homozygous mutation in the carboxyl-propeptide-coding region of the pro alpha 2(I) collagen gene in a patient with osteogenesis imperfecta.Proceedings of the National Academy of Sciences, 1984
- Isolation of biologically active ribonucleic acid from sources enriched in ribonucleaseBiochemistry, 1979