Ngo J T, Bateman J B, Spence M A, Cortessis V, Sparkes R S, Kivlin J D, Mohandas T, Inana G
Vision Genetics Center, Jules Stein Eye Institute, Los Angeles, California 90024.
Genomics. 1990 Jan;6(1):123-8. doi: 10.1016/0888-7543(90)90456-5.
A human ornithine aminotransferase (OAT) locus has been mapped to the Xp11.2, as has the Norrie disease locus. We used a cDNA probe to investigate a 3-generation UCLA family with Norrie disease; a 4.2-kb RFLP was detected and a maximum lod score of 0.602 at zero recombination fraction was calculated. We used the same probe to study a second multigeneration family with Norrie disease from Utah. A different RFLP of 7.5 kb in size was identified and a recombinational event between the OAT locus represented by this RFLP and the disease loci was observed. Linkage analysis of these two loci in this family revealed a maximum load score of 1.88 at a recombination fraction of 0.10. Although both families have affected members with the same disease, the lod scores are reported separately because the 4.2- and 7.5-kb RFLPs may represent two different loci for the X-linked OAT.