TY  - GEN
AU  - Hanein,Sylvain
AU  - Perrault,Isabelle
AU  - Olsen,Päivi
AU  - Lopponen,Tuija
AU  - Hietala,Marja
AU  - Gerber,Sylvie
AU  - Jeanpierre,Marc
AU  - Barbet,Fabienne
AU  - Ducroq,Dominique
AU  - Hakiki,Sélim
AU  - Munnich,Arnold
AU  - Rozet,Jean-Michel
AU  - Kaplan,Josseline
TI  - Evidence of a founder effect for the RETGC1 (GUCY2D) 2943DelG mutation in Leber congenital amaurosis pedigrees of Finnish origin
SN  - 1098-1004
PY  - 2003///0103
KW  - Blindness
KW  - congenital
KW  - Cyclic GMP
KW  - metabolism
KW  - Female
KW  - Finland
KW  - Founder Effect
KW  - Guanine
KW  - Guanylate Cyclase
KW  - genetics
KW  - Humans
KW  - Linkage Disequilibrium
KW  - Male
KW  - Mutation
KW  - Nuclear Family
KW  - Optic Atrophies, Hereditary
KW  - enzymology
KW  - Pedigree
KW  - Polymorphism, Single Nucleotide
KW  - Sequence Deletion
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/humu.9067
ER  -