<p>Summary of the known congenital cataract causing mutations in the <i>EPHA2</i> gene.</p
The aim of this study was to investigate the mutation spectrum and frequency of 34 known genes in 18...
<div><p>Purpose</p><p>The aim of this study was to investigate the mutation spectrum and frequency o...
Congenital cataracts can occur as a non-syndromic isolated ocular disease or as a part of genetic sy...
<p>Summary of mutations identified in <i>LIM2</i> associated with cataractogenesis.</p
Background: Congenital cataract is a rare disorder characterized by crystallin denaturation, which b...
Purpose: Congenital cataract is a leading cause of childhood blindness. Mutations in the EPHA2 gene ...
<div><p>Congenital cataract is the most common cause of treatable visual impairment in children worl...
Congenital cataract is the most common cause of treatable visual impairment in children worldwide. M...
This is an open-access article distributed under the terms of the Creative Commons Attribution Licen...
Congenital cataracts are the prime cause for irreversible blindness in children. The global incidenc...
Pediatric cataracts are observed in 1-15 per 10,000 births with 10-25 % of cases attributed to genet...
Purpose: The aim of this study was to investigate the mutation spectrum and frequency of 34 known ge...
PURPOSE: The aim of this study was to investigate the mutation spectrum and frequency of 34 known ge...
AIM: To summarize the phenotypes and identify the underlying genetic cause of the CRYBB1 and CRYBB2 ...
The present study aimed to identify the genetic mutations in two families affected with congenital c...
The aim of this study was to investigate the mutation spectrum and frequency of 34 known genes in 18...
<div><p>Purpose</p><p>The aim of this study was to investigate the mutation spectrum and frequency o...
Congenital cataracts can occur as a non-syndromic isolated ocular disease or as a part of genetic sy...
<p>Summary of mutations identified in <i>LIM2</i> associated with cataractogenesis.</p
Background: Congenital cataract is a rare disorder characterized by crystallin denaturation, which b...
Purpose: Congenital cataract is a leading cause of childhood blindness. Mutations in the EPHA2 gene ...
<div><p>Congenital cataract is the most common cause of treatable visual impairment in children worl...
Congenital cataract is the most common cause of treatable visual impairment in children worldwide. M...
This is an open-access article distributed under the terms of the Creative Commons Attribution Licen...
Congenital cataracts are the prime cause for irreversible blindness in children. The global incidenc...
Pediatric cataracts are observed in 1-15 per 10,000 births with 10-25 % of cases attributed to genet...
Purpose: The aim of this study was to investigate the mutation spectrum and frequency of 34 known ge...
PURPOSE: The aim of this study was to investigate the mutation spectrum and frequency of 34 known ge...
AIM: To summarize the phenotypes and identify the underlying genetic cause of the CRYBB1 and CRYBB2 ...
The present study aimed to identify the genetic mutations in two families affected with congenital c...
The aim of this study was to investigate the mutation spectrum and frequency of 34 known genes in 18...
<div><p>Purpose</p><p>The aim of this study was to investigate the mutation spectrum and frequency o...
Congenital cataracts can occur as a non-syndromic isolated ocular disease or as a part of genetic sy...
DOI
Add to ORKG