AIM: To investigate a Chinese autosomal dominant congenital cataract(ADCC)family and to find the relationship between the candidate gene and this pedigree. METHODS: The clinical data and blood samples of the ADCC family were collected.Microsatellite markers were chosen according to 24 known candidate genes of ADCC. Lod scores of microsatellite markers were calculated with Mlink package of linkage software. RESULTS: The phenotype of this family was nuclear cataract. After linkage analyzing,Lod scores of 50 microsatellite markers were less than zero. There was no linkage between the microsatellite markers and this pedigree.CONCLUSION: The related gene of this family is not among the known genes of ADCC maybe there is a new pathogenic gene in ...
7 páginas, 1 figura, 2 tablas.-- Licence Creative Commons, attribution, Non-commercial licence.-- et...
Congenital cataract is a clinically and genetically heterogeneous disease. The present study was und...
Purpose. To screen out pathogenic genes in a Chinese family with congenital cataract and iris colobo...
AIM: To map the causal gene of congenital nuclear cataract in a family in the area of northeast.METH...
Congenital cataracts are one of the leading causes of visual impairment and blindness in children, a...
Purpose: To map a gene responsible for infantile cataract in a large four-generation, non- consangui...
The aim of this study was to investigate the mutation spectrum and frequency of 34 known genes in 18...
Purpose: Through homozygosity mapping and linkage analysis, our aim is finding a cataract locus whic...
Purpose To determine by linkage analysis the chromosomal locus responsible for autosomal dominant co...
Aim: The aims of this study are to assess the clinical heterogeneity of autosomal dominant cataract ...
AimsThe study aims to detect the underlying genetic defect in two autosomal dominant congenital cata...
Purpose: The aim of this study was to investigate the mutation spectrum and frequency of 34 known ge...
AimsThe study aims to detect the underlying genetic defect in two autosomal dominant congenital cata...
PURPOSE: The aim of this study was to investigate the mutation spectrum and frequency of 34 known ge...
AIM: To identify the disease-causing mutation responsible for the presence of congenital cataract in...
7 páginas, 1 figura, 2 tablas.-- Licence Creative Commons, attribution, Non-commercial licence.-- et...
Congenital cataract is a clinically and genetically heterogeneous disease. The present study was und...
Purpose. To screen out pathogenic genes in a Chinese family with congenital cataract and iris colobo...
AIM: To map the causal gene of congenital nuclear cataract in a family in the area of northeast.METH...
Congenital cataracts are one of the leading causes of visual impairment and blindness in children, a...
Purpose: To map a gene responsible for infantile cataract in a large four-generation, non- consangui...
The aim of this study was to investigate the mutation spectrum and frequency of 34 known genes in 18...
Purpose: Through homozygosity mapping and linkage analysis, our aim is finding a cataract locus whic...
Purpose To determine by linkage analysis the chromosomal locus responsible for autosomal dominant co...
Aim: The aims of this study are to assess the clinical heterogeneity of autosomal dominant cataract ...
AimsThe study aims to detect the underlying genetic defect in two autosomal dominant congenital cata...
Purpose: The aim of this study was to investigate the mutation spectrum and frequency of 34 known ge...
AimsThe study aims to detect the underlying genetic defect in two autosomal dominant congenital cata...
PURPOSE: The aim of this study was to investigate the mutation spectrum and frequency of 34 known ge...
AIM: To identify the disease-causing mutation responsible for the presence of congenital cataract in...
7 páginas, 1 figura, 2 tablas.-- Licence Creative Commons, attribution, Non-commercial licence.-- et...
Congenital cataract is a clinically and genetically heterogeneous disease. The present study was und...
Purpose. To screen out pathogenic genes in a Chinese family with congenital cataract and iris colobo...