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Ser186Pro mutation of RHO gene in a Spanish autosomal dominant retinitis pigmentosa (ADRP) family

Authors :
M J, Trujillo
B, Garcia-Sandoval
I, Lorda-Sanchez
A, Gimenez
R, Sanz
Rodriguez de Alba M
M C, Gonzalez-Gonzalez
A, Ibañez
C, Ramos
C, Ayuso
Source :
Ophthalmic genetics. 21(4)
Publication Year :
2001

Abstract

A Spanish family affected with autosomal dominant retinitis pigmentosa (ADRP) with a diffuse phenotype showed a mutation in the rhodopsin gene. The mutation was the transition T--C in codon 186, which has been reported once before in an American patient (Dryja et al., Proc Natl Acad Sci USA 1991;88:9370-9374). This change replaces a serine by a proline in the second intradiscal loop of the protein, generating a molecule that is probably folding- and transport-defective.

Details

ISSN :
13816810 and 93709374
Volume :
21
Issue :
4
Database :
OpenAIRE
Journal :
Ophthalmic genetics
Accession number :
edsair.pmid..........c23ccee2296afac684221be9d900ee8b