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Evidence of a founder effect for the RETGC1 (GUCY2D) 2943DelG mutation in Leber congenital amaurosis pedigrees of Finnish origin
Author(s) -
Hanein Sylvain,
Perrault Isabelle,
Olsen Päivi,
Lopponen Tuija,
Hietala Marja,
Gerber Sylvie,
Jeanpierre Marc,
Barbet Fabienne,
Ducroq Dominique,
Hakiki Sélim,
Munnich Arnold,
Rozet JeanMichel,
Kaplan Josseline
Publication year - 2002
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/humu.9067
Subject(s) - gucy2d , biology , genetics , founder effect , pedigree chart , haplotype , mutation , gene , genetic heterogeneity , point mutation , phenotype , genotype , receptor , guanylate cyclase , guanylate cyclase 2c
Leber congenital amaurosis (LCA) is the earliest and most severe form of all inherited retinal dystrophies. It is a genetically heterogeneous condition as six disease‐causing genes have been hitherto identified. Among them, RETGC1 (GUCY2D), is more frequently implicated in our series of LCA patients. Interestingly, 70 % of the families with RETGC1 mutations are originating from Mediterranean countries, the remaining families (30%) being originating from various countries across the world. Here, we report, the identification of the same homozygous RETGC1 non‐sens mutation in three unrelated and non‐consanguineous LCA families of Finnish origin, suggesting a founder effect. Interestingly, no linkage desequilibrium was found using polymorphic markers flanking the RETGC1 gene, supporting the view that the mutation is very ancient. Haplotype studies and Bayesian calculation point the founder mutation to 150 generations (95% credible interval 80‐240 generations), i.e., 3000 years ago. © 2002 Wiley‐Liss, Inc.