Rosenberg L E
Science. 1966 Dec 9;154(3754):1341-3. doi: 10.1126/science.154.3754.1341.
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.
对来自三个无亲缘关系家系的四名形成结石的胱氨酸尿症患者的研究表明,每个人都是导致胱氨酸尿症的三个已描述突变基因(I、II、III)中的两个的杂合子。他们的基因型分别为I-II、II-III、I-III和I-III。这些双重杂合子患者在表型上与基因型为I-I、II-I或III-III的胱氨酸尿症纯合子无法区分。这些数据提供了首个直接证据,证明所有已知的导致胱氨酸尿症遗传异质性的突变都是等位基因。