PurposeTo identify specific mutations causing North Carolina macular dystrophy (NCMD).DesignWhole-genome sequencing coupled with reverse transcription polymerase chain reaction (RT-PCR) analysis of gene expression in human retinal cells.ParticipantsA total of 141 members of 12 families with NCMD and 261 unrelated control individuals.MethodsGenome sequencing was performed on 8 affected individuals from 3 families affected with chromosome 6–linked NCMD (MCDR1) and 2 individuals affected with chromosome 5–linked NCMD (MCDR3). Variants observed in the MCDR1 locus with frequencies <1% in published databases were confirmed using Sanger sequencing. Confirmed variants absent from all published databases were sought in 8 additional MCDR1 families an...
Inherited retinal diseases (IRDs) are a group of genetically and phenotypically heterogenous disorde...
Retinal dystrophies are a heterogeneous group of diseases that lead to either partial or complete bl...
To assess the clinical utility of targeted Next-Generation Sequencing (NGS) for the diagnosis of Inh...
PurposeTo identify specific mutations causing North Carolina macular dystrophy (NCMD).DesignWhole-ge...
Publisher Copyright: © 2017 The Author(s).Autosomal dominant North Carolina macular dystrophy (NCMD)...
BACKGROUND: Developmental macular disorders are a heterogeneous group of rare retinal conditions tha...
AbstractNorth Carolina macular dystrophy (NCMD) is an autosomal dominant macular disease, was mapped...
North Carolina macular dystrophy (NCMD) is a rare autosomal-dominant disease affecting macular devel...
North Carolina macular dystrophy (NCMD) is a rare autosomal dominant disease affecting macular devel...
Purpose: To clinically and molecularly investigate a new family with North Carolina macular dystroph...
<p><i>Background</i>: Developmental macular disorders are a heterogeneous group of rare retinal cond...
Autosomal dominant North Carolina macular dystrophy (NCMD) is believed to represent a failure of mac...
Inherited retinal dystrophies (RDs) are a clinically heterogeneous group of eye diseases that result...
International audienceIn this study, we report a novel duplication causing North Carolina macular dy...
PURPOSE: To identify, using genome sequencing (GS), likely pathogenic non-coding variants in inherit...
Inherited retinal diseases (IRDs) are a group of genetically and phenotypically heterogenous disorde...
Retinal dystrophies are a heterogeneous group of diseases that lead to either partial or complete bl...
To assess the clinical utility of targeted Next-Generation Sequencing (NGS) for the diagnosis of Inh...
PurposeTo identify specific mutations causing North Carolina macular dystrophy (NCMD).DesignWhole-ge...
Publisher Copyright: © 2017 The Author(s).Autosomal dominant North Carolina macular dystrophy (NCMD)...
BACKGROUND: Developmental macular disorders are a heterogeneous group of rare retinal conditions tha...
AbstractNorth Carolina macular dystrophy (NCMD) is an autosomal dominant macular disease, was mapped...
North Carolina macular dystrophy (NCMD) is a rare autosomal-dominant disease affecting macular devel...
North Carolina macular dystrophy (NCMD) is a rare autosomal dominant disease affecting macular devel...
Purpose: To clinically and molecularly investigate a new family with North Carolina macular dystroph...
<p><i>Background</i>: Developmental macular disorders are a heterogeneous group of rare retinal cond...
Autosomal dominant North Carolina macular dystrophy (NCMD) is believed to represent a failure of mac...
Inherited retinal dystrophies (RDs) are a clinically heterogeneous group of eye diseases that result...
International audienceIn this study, we report a novel duplication causing North Carolina macular dy...
PURPOSE: To identify, using genome sequencing (GS), likely pathogenic non-coding variants in inherit...
Inherited retinal diseases (IRDs) are a group of genetically and phenotypically heterogenous disorde...
Retinal dystrophies are a heterogeneous group of diseases that lead to either partial or complete bl...
To assess the clinical utility of targeted Next-Generation Sequencing (NGS) for the diagnosis of Inh...