Volume 6, Issue 1 pp. 131-136
Original Article
Full Access

Combined segregation and linkage analysis for IDDM and HLA-DR under several ascertainment assumptions

Leigh Pascoe

Corresponding Author

Leigh Pascoe

Genetic Epidemiology Department, Memorial Sloan Kettering Cancer Center

Dept. Pediatrics, Cornell Medical Center, 515 E 71 S613, New York, NY 10021Search for more papers by this author
Stephanie Sherman

Stephanie Sherman

Genetic Epidemiology Department, Memorial Sloan Kettering Cancer Center

Search for more papers by this author
Danny Wu

Danny Wu

Genetic Epidemiology Department, Memorial Sloan Kettering Cancer Center

Search for more papers by this author
Murray Becker

Murray Becker

Genetic Epidemiology Department, Memorial Sloan Kettering Cancer Center

Search for more papers by this author
Catherine Falk

Catherine Falk

New York Blood Center

Search for more papers by this author
First published: 1989
Citations: 7

Abstract

Combined segregation and linkage analysis of the Genetic Analysis Workshop 5 (GAW5) data suggests a complex basis for susceptibility to insulin-dependent diabetes mellitus (IDDM). One susceptibility gene, linked to the HLA-DR region, is additive on the liability scale (d = .49 ± .15,t = 2.9 ± .6) with a gene frequency q = .30 ± .03. A second locus, with a gene frequency of q = .07 ± .02, which is recessive and unlinked to HLA, is also suggested by the analysis. The ascertainment correction used has little effect on the results, presumably because most of the information comes from the cosegregation of HLA alleles and disease status. The results are consistent with a direct involvement of the HLA-DR region in susceptibility, but are not a proof of it.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.