Pages that link to "Q28205386"

The following pages link to Mutations in the CACNA1F and NYX genes in British CSNBX families (Q28205386):

Displaying 21 items.

• Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein trafficking (Q24301599) (← links)
• Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness (Q24301994) (← links)
• A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation. (Q24302179) (← links)
• X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene (Q24305973) (← links)
• Mutations in NYX of individuals with high myopia, but without night blindness (Q24653288) (← links)
• (Q28161065) (redirect page) (← links)
• CSNB1 in Chinese families associated with novel mutations in NYX (Q28238064) (← links)
• Modified Ca(v)1.4 expression in the Cacna1f(nob2) mouse due to alternative splicing of an ETn inserted in exon 2 (Q28473025) (← links)
• Congenital stationary night blindness and a "Schubert-Bornschein" type electrophysiology in a family with dominant inheritance (Q33204820) (← links)
• A novel large in-frame deletion within the CACNA1F gene associates with a cone-rod dystrophy 3-like phenotype (Q35016967) (← links)
• Retinal dysfunction and refractive errors: an electrophysiological study of children. (Q35593091) (← links)
• In vivo analysis of voltage-dependent calcium channels (Q35682326) (← links)
• Sequence variations of GRM6 in patients with high myopia. (Q37395103) (← links)
• IkappaB kinase beta phosphorylates Dok1 serines in response to TNF, IL-1, or gamma radiation (Q37713955) (← links)
• Retinoschisin Facilitates the Function of L-Type Voltage-Gated Calcium Channels (Q41334192) (← links)
• Congenital stationary night blindness associated with mutations in GRM6 encoding glutamate receptor MGluR6. (Q42842209) (← links)
• A comparison of ERG abnormalities in XLRS and XLCSNB. (Q45084226) (← links)
• X-linked infantile periodic alternating nystagmus. (Q53577798) (← links)
• Mutations in RPGR and RP2 of Chinese patients with X-linked retinitis pigmentosa. (Q54449556) (← links)
• Isolation and characterization of the leucine-rich proteoglycan nyctalopin gene (cNyx) from chick. (Q54633110) (← links)
• Is optic nerve fibre mis-routing a feature of congenital stationary night blindness? (Q82757815) (← links)