References
Astrin, K.H., Warner, C.A., Yoo, H.W., Goodfellow, P.J., Tsai, S.F., Desnick, R.J. (1991). Regional assignment of the human uroporphyrinogen III synthase (URO S) gene to chromosome 10q25.2–q26.3. Hum. Genet. 87, 18–22.
Boulechfar, S., Da Silva, V., Deybach, J.C., Nordmann, Y., Grandchamp, B., Verneuil, H. de (1992). Heterogeneity of the mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria. Hum. Genet. 88, 320–324.
Deybach, J.C., Verneuil, H. de, Boulechfar, S., Grandchamp, B., Nordmann, Y. (1990). Point mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria (Günther's disease). Blood 75, 1763–1765.
Jordan, P.M., Mgbeje, B.I.A., Thomas, S.D., Alwan, A.F. (1988). Nucleotide sequence of the hemD gene of Escherichia coli encoding uroporphyrinogen III synthase and initial evidence for a hem operon. Biochem. J. 249, 613–616.
Kappas, A., Sassa, S., Galbraith, R.A., Nordmann, Y. (1989). The porphyrias. In The Metabolic Basis of Inherited Disease C.R. Scriver, A.L. Beaudet, W.S. Sly, D. Valle, eds. (New York: McGraw Hill), pp. 1305–1365.
Montagutelli, X. (1990). GENE-LINK: a program in PASCAL for back-cross genetic linkage analysis. J. Hered. 81, 490–491.
O'Brien, S.J., Marshall Graves, J.A. (1991). Report of the comparative committee for human, mouse and other rodents. Cytogenet. Cell Genet. 58, 1152–1189.
O'Brien, S.J., Womack, K.E., Lyons, L.A., Moore, K.J., Jenkins, N.A., Copeland, N.G. (1993). Anchored reference loci for comparative genome mapping in mammals. Nature Genet. 3, 103–112.
Orita, M., Iwahana, H., Kanazawa, H., Hayashi, K., Sekiya, T. (1989). Detection of polymorphisms of human DNA by gel electrophoresis as single-stranded conformation polymorphisms. Proc. Natl. Acad. Sci. USA 86, 2766–2770.
Sambrook J., Fritsch, E.F., Maniatis, T. (1989) Molecular Cloning: A Laboratory Manual. Eds.: Ford N., Nolan C., Ferguson, M., (Cold Spring Harbor, N.Y.: Cold Spring Harbor Laboratory Press).
Serikawa, T., Montagutelli, X., Simon-Chazottes, D., Guénet, J-L. (1992). Polymorphisms revealed by PCR with short-sized, arbitrary primers are reliable markers for mouse and rat gene mapping. Mamm. Genome 3, 65–72.
Smithies, O. (1993). Animal models of human genetic diseases. Trends Genet. 9, 112–116.
Tsaï, S.F., Bishop, D.F., Desnick, R.J. (1988). Human UROIIIS: molecular cloning, nucleotide sequence and expression of a full-length cDNA. Proc. Natl. Acad. Sci. USA 85, 7049–7053.
Warner, C.A., Yoo, H.W., Roberts, A.G., Desnick, R.J. (1992). Congenital erythropoietic porphyria: identification and expression of exonic mutations in the uroporphyrinogen III synthase gene. J. Clin. Invest. 89, 693–700.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Bensidhoum, M., Ged, C.M., Poirier, C. et al. The cDNA sequence of mouse uroporphyrinogen III synthase and assignment to mouse Chromosome 7. Mammalian Genome 5, 728–730 (1994). https://doi.org/10.1007/BF00426082
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00426082