Pages that link to "Q39704029"

The following pages link to Correlation between electroretinogram findings and molecular analysis in the Duchenne muscular dystrophy phenotype. (Q39704029):

Displaying 14 items.

• Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness (Q21710708) (← links)
• The electroretinographic diagnosis of the incomplete form of congenital stationary night blindness (Q24312225) (← links)
• Duchenne muscular dystrophy: negative electroretinograms and normal dark adaptation. Reappraisal of assignment of X linked incomplete congenital stationary night blindness (Q33676559) (← links)
• ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy (Q35432074) (← links)
• Red-green color vision impairment in Duchenne muscular dystrophy (Q35788517) (← links)
• X linked retinoschisis (Q37313589) (← links)
• Mouse b-wave mutants (Q38176282) (← links)
• Distinct synaptic localization patterns of brefeldin A-resistant guanine nucleotide exchange factors BRAG2 and BRAG3 in the mouse retina (Q39754713) (← links)
• alpha-dystroglycan isoforms are differentially distributed in adult rat retina (Q40831877) (← links)
• Electroretinographic findings in Duchenne/Becker muscular dystrophy and correlation with genotype (Q44153486) (← links)
• The electroretinographic phenotype of dogs with Golden Retriever muscular dystrophy (Q49156079) (← links)
• Autosomal dominant inheritance of a negative electroretinogram phenotype in three generations. (Q52137076) (← links)
• Electroretinogram in Duchenne/Becker muscular dystrophy (Q74551770) (← links)
• Single-transcript multiplex in situ hybridisation reveals unique patterns of dystrophin isoform expression in the developing mammalian embryo (Q98159750) (← links)