| Literature DB >> 16374045 |
Jac C Charlesworth1, James M Stankovich, David A Mackey, Jamie E Craig, Michael Haybittel, Rodney N Westmore, Michèle M Sale.
Abstract
Primary open-angle glaucoma (POAG) is genetically heterogeneous, with 6 named POAG loci GLC1A-F mapped and genes myocilin (MYOC) and optineurin (OPTN) identified at 2 of the loci. Using penetrance-model-free methods, we screened the POAG loci GLC1A-F in an extended Australian pedigree, using 3-5 markers within each locus. p values of less than 0.05 were obtained empirically using SimWalk2 and exactly using Genehunter for 2 markers within the GLC1B region on chromosome 2. Fine mapping of this region produced p values of 0.01 or less at 5 markers flanked by D2S1897 and D2S2269. The 9 cM haplotype of interest overlaps the original GLC1B region. These results provide supportive evidence for the GLC1B locus on chromosome 2cen-q13 and verify the existence of POAG susceptibility gene in this region, increasing the likelihood of gene identification. 2006 S. Karger AG, BaselEntities:
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Year: 2006 PMID: 16374045 DOI: 10.1159/000089271
Source DB: PubMed Journal: Ophthalmologica ISSN: 0030-3755 Impact factor: 3.250