1 - 25 of 2
Number of results to display per page
TitleDateType
1 Autosomal dominant cone dystrophy caused by a novel mutation in the GCAP1 gene (GUCA1A)2005Text
2 Loss of ER retention and sequestration of the wild-type ELOVL4 by Stargardt disease dominant negative mutants2005Text
1 - 25 of 2