Pages that link to "Q76292853"
Jump to navigation
Jump to search
The following pages link to [Analysis of the human electroretinogram] (Q76292853):
Displaying 50 items.
- Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness (Q21710708) (← links)
- Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness (Q24290479) (← links)
- The electroretinographic diagnosis of the incomplete form of congenital stationary night blindness (Q24312225) (← links)
- An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness (Q24315182) (← links)
- Missense mutation in the gene encoding the alpha subunit of rod transducin in the Nougaret form of congenital stationary night blindness (Q24328892) (← links)
- Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1 (Q24517919) (← links)
- Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6 (Q24555742) (← links)
- Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus) (Q24644487) (← links)
- Genotype-phenotype correlation in British families with X linked congenital stationary night blindness (Q24671479) (← links)
- A Naturally Occurring Canine Model of Autosomal Recessive Congenital Stationary Night Blindness (Q27320207) (← links)
- The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein (Q28142943) (← links)
- Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB) (Q28594570) (← links)
- Congenital stationary night blindness and a "Schubert-Bornschein" type electrophysiology in a family with dominant inheritance (Q33204820) (← links)
- SURGICAL EXPERIENCES WITH THROMBOCYTOPENIC PATIENTS (Q33355341) (← links)
- Night vision in a case of vitamin A deficiency due to malabsorption (Q33642343) (← links)
- Pupillary constriction to darkness (Q33643970) (← links)
- The Briard dog: a new animal model of congenital stationary night blindness (Q33647457) (← links)
- TRPM1 mutations are associated with the complete form of congenital stationary night blindness (Q33728459) (← links)
- Rod pathways: the importance of seeing nothing (Q33756115) (← links)
- Spectrum of Cav1.4 dysfunction in congenital stationary night blindness type 2 (Q33786236) (← links)
- Photopic ON- and OFF-pathway abnormalities in retinal dystrophies (Q34164016) (← links)
- A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness (Q34169360) (← links)
- Congenital stationary nightblindness (Q34208689) (← links)
- A study of the visual functions in patients with retinal pigmentary degeneration following the use of NP 207 (Q34229330) (← links)
- Problems of peripheral vision (Q34247312) (← links)
- Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness (Q34318093) (← links)
- The negative ERG is not synonymous with nightblindness (Q34331164) (← links)
- Assessment of night vision problems in patients with congenital stationary night blindness (Q34712842) (← links)
- TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness (Q35011677) (← links)
- A novel large in-frame deletion within the CACNA1F gene associates with a cone-rod dystrophy 3-like phenotype (Q35016967) (← links)
- Diagnostic ophthalmology. Congenital stationary night blindness (CSNB) (Q35110901) (← links)
- NYX mutations in four families with high myopia with or without CSNB1 (Q35169701) (← links)
- Autofluorescence imaging and spectral-domain optical coherence tomography in incomplete congenital stationary night blindness and comparison with retinitis pigmentosa (Q35225965) (← links)
- A novel p.Gly603Arg mutation in CACNA1F causes Åland island eye disease and incomplete congenital stationary night blindness phenotypes in a family (Q35629094) (← links)
- GNAT1 associated with autosomal recessive congenital stationary night blindness (Q35921448) (← links)
- Assessing retinal structure in complete congenital stationary night blindness and Oguchi disease (Q36400102) (← links)
- Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation (Q36533292) (← links)
- Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness (Q36903762) (← links)
- Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics (Q36980803) (← links)
- Photoreceptor and postreceptor responses in congenital stationary night blindness (Q37012780) (← links)
- Cone dystrophies with negative photopic electroretinogram (Q37302028) (← links)
- Molecular profiling of complete congenital stationary night blindness: a pilot study on an Indian cohort (Q37656373) (← links)
- LRIT3 Differentially Affects Connectivity and Synaptic Transmission of Cones to ON- and OFF-Bipolar Cells (Q37731913) (← links)
- Pleiotropic effects of pigmentation genes in horses (Q37808732) (← links)
- Negative electroretinograms in the pediatric and adult population (Q37975929) (← links)
- Long-Term Clinical Course in a Patient with Complete Congenital Stationary Night Blindness. (Q38781808) (← links)
- Rod densitometry in night blindness: a review and two puzzling cases. Rod densitometry in night blindness (Q39513741) (← links)
- Undetectable S cone electroretinogram b-wave in complete congenital stationary night blindness (Q39719773) (← links)
- New electroretinographic findings obtained in congenital forms of dyschromatopsia (Q39835624) (← links)
- In vivo release and retinal toxicity of cyclosporine-loaded intravitreal device (Q40312824) (← links)