Cystinuria: Genetic Heterogeneity and Allelism
- 9 December 1966
- journal article
- research article
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 154 (3754), 1341-1343
- https://doi.org/10.1126/science.154.3754.1341
Abstract
Studies of four stoneforming cystinuric subjects from three unrelated pedigrees indicated that each was heterozygous for two of the three described mutant genes producing cystinuria ( I, II, III). Their genotypes were I-II, II-III, I-III, and I-III, respectively. These doubly heterozygous patients were phenotypically indistinguishable from cystinuric homozygotes of genotype I-I, II-I, or III-III. The data provide the first direct evidence that all of the known mutations responsible for the genetic heterogeneity in cystinuria are allelic.This publication has 5 references indexed in Scilit:
- Cystinuria: biochemical evidence for three genetically distinct diseases.Journal of Clinical Investigation, 1966
- Heterozygotes for cystinuriaAnnals of Human Genetics, 1966
- Cystinuria: In vitro Demonstration of an Intestinal Transport DefectScience, 1964
- PHENOTYPES AND GENOTYPES IN CYSTINURIAAnnals of Human Genetics, 1955
- THE PATTERN OF AMINO‐ACID EXCRETION IN CYSTINURIAAnnals of Human Genetics, 1955