To identify the molecular basis of non-syndromic autosomal recessive congenital cataracts (arCC) in a consanguineous family. in a mouse model., which was detected in the mouse lens as early as embryonic day 15 (E15) increased after birth to a level that was sustained through the postnatal time points. is responsible for autosomal recessive congenital cataracts
During an ethylnitrosourea mutagenesis screen. Aey5, a new mouse mutation exhibiting an autosomal do...
peer reviewedDuring an ethylnitrosourea mutagenesis screen, Aey5, a new mouse mutation exhibiting an...
Congenital cataracts can occur as a non-syndromic isolated ocular disease or as a part of genetic sy...
This study was initiated to identify causal mutations responsible for autosomal recessive congenital...
<div><p>Purpose</p><p>To identify the molecular basis of non-syndromic autosomal recessive congenita...
To identify the molecular basis of non-syndromic autosomal recessive congenital cataracts (arCC) in ...
PurposeTo investigate the genetic basis of autosomal recessive congenital cataracts (arCC) in a larg...
The aim of this study is to identify the molecular basis of autosomal recessive congenital cataracts...
Much of our knowledge about the function of genes in cataracts has been derived from the molecular a...
The clinical and histologic features are reported of an autosomal dominant mouse cataract that was f...
Purpose: Through homozygosity mapping and linkage analysis, our aim is finding a cataract locus whic...
Cataracts (opacities of the lens) are frequent in the elderly, but rare in paediatric practice. Cong...
Opacities of the eye lens (cataracts) are well known as congenital (and mainly hereditary) disorders...
<div><p>Purpose</p><p>This study was performed to investigate the genetic determinants of autosomal ...
A mouse mutant expressing a bilateral nuclear and radial cataract was found after paternal treatment...
During an ethylnitrosourea mutagenesis screen. Aey5, a new mouse mutation exhibiting an autosomal do...
peer reviewedDuring an ethylnitrosourea mutagenesis screen, Aey5, a new mouse mutation exhibiting an...
Congenital cataracts can occur as a non-syndromic isolated ocular disease or as a part of genetic sy...
This study was initiated to identify causal mutations responsible for autosomal recessive congenital...
<div><p>Purpose</p><p>To identify the molecular basis of non-syndromic autosomal recessive congenita...
To identify the molecular basis of non-syndromic autosomal recessive congenital cataracts (arCC) in ...
PurposeTo investigate the genetic basis of autosomal recessive congenital cataracts (arCC) in a larg...
The aim of this study is to identify the molecular basis of autosomal recessive congenital cataracts...
Much of our knowledge about the function of genes in cataracts has been derived from the molecular a...
The clinical and histologic features are reported of an autosomal dominant mouse cataract that was f...
Purpose: Through homozygosity mapping and linkage analysis, our aim is finding a cataract locus whic...
Cataracts (opacities of the lens) are frequent in the elderly, but rare in paediatric practice. Cong...
Opacities of the eye lens (cataracts) are well known as congenital (and mainly hereditary) disorders...
<div><p>Purpose</p><p>This study was performed to investigate the genetic determinants of autosomal ...
A mouse mutant expressing a bilateral nuclear and radial cataract was found after paternal treatment...
During an ethylnitrosourea mutagenesis screen. Aey5, a new mouse mutation exhibiting an autosomal do...
peer reviewedDuring an ethylnitrosourea mutagenesis screen, Aey5, a new mouse mutation exhibiting an...
Congenital cataracts can occur as a non-syndromic isolated ocular disease or as a part of genetic sy...