volume 16, issue 11, P1134-1141 1997
DOI: 10.1076/ceyr.16.11.1134.5099
View full text
|
|
Share

Abstract: . These findings indicate that the degree of change in the secondary structure of peripherin/RDS can explain in part the correlation between genotype and phenotype in autosomal-dominant retinal degeneration associated with missense mutations in the peripherin/RDS gene.