Mcllraith would be pleased — one hundred years after his documentation of nephrogenic diabetes insipidus, the pursuit of the molecular pathology behind this condition has finally succeeded.
Article PDF
References
Mcllraith, C. H. et al. Lancet II, 767 (1892).
van den Ouweland, A. M. W. et al. Nature Genet. 2, 99–102 (1992).
Pang, Y. et al. Nature Genet. 2, 103–106 (1992).
Sharif, M. & Hanley, M. R. Nature 357, 279–280 (1992).
Warren, S. T. Dysmorph. clin. Genet. (in the press).
Birnbaumer, M. et al. Nature 357, 333–335 (1992).
Lolait, S. J. et al. Nature 357, 336–339 (1992).
Rosenthal, W. et al. Nature 359, 233–235 (1992).
Rosenfeld, P. L. et al. Nature Genet. 1, 209–213 (1992).
Rights and permissions
About this article
Cite this article
Davies, K. Diabetes defect defined. Nature 359, 434 (1992). https://doi.org/10.1038/359434a0
Issue Date:
DOI: https://doi.org/10.1038/359434a0
This article is cited by
-
Expression studies of two vasopressin V2 receptor gene mutations, R202C and 804insG, in nephrogenic diabetes insipidus
Kidney International (1995)
-
A molecular approach to inherited kidney disorders
Kidney International (1993)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.