Analysis of the mutations of rhodopsin gene in autosomal dominant retinitis pigmentosa family / 中华眼底病杂志
Chinese Journal of Ocular Fundus Diseases
; (6)2000.
Article
en Zh
| WPRIM
| ID: wpr-520026
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WPRO
ABSTRACT
Objective To detect and analyse the mutations in rhodopsin gene of members in a family affected by autosomal dominant retinitis pigmentosa (ADRP). Methods Using the polymerase chain reaction (PCR), we amplified exon 1-5 of rhodopsin gene in patients with ADRP,and analyzed it with direct sequence measuement. Results The Gly-182-Asp mutation in the rhodopsin gene was detected in most of affected members of this ADRP family, but no mutation was detected in two affected members and the control ones. Conclusion We cannot regard the Gly-182-Asp mutation in the rhodopsin gene as the pathagenic factor of the ADRP family. It is likely there is a new gene next to the rhodopsin gene.
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WPRIM
Idioma:
Zh
Revista:
Chinese Journal of Ocular Fundus Diseases
Año:
2000
Tipo del documento:
Article