These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
117 related articles for article (PubMed ID: 37212526)
1. Rod-cone dystrophy in an adult with GNB1-related disorder: An expansion of the phenotype and natural history. Yang XR; Kassam F; Innes AM Am J Med Genet C Semin Med Genet; 2023 Jun; 193(2):183-187. PubMed ID: 37212526 [TBL] [Abstract][Full Text] [Related]
2. Association of the Asn306Ser variant of the SP4 transcription factor and an intronic variant in the beta-subunit of transducin with digenic disease. Gao YQ; Danciger M; Ozgul RK; Gribanova Y; Jacobson S; Farber DB Mol Vis; 2007 Feb; 13():287-92. PubMed ID: 17356515 [TBL] [Abstract][Full Text] [Related]
3. Retinitis pigmentosa and bilateral cystoid macular oedema in a patient heterozygous for the RIM1 mutation previously associated with cone-rod dystrophy 7. Warwick AN; Shawkat F; Lotery AJ Ophthalmic Genet; 2017; 38(2):178-182. PubMed ID: 27176872 [TBL] [Abstract][Full Text] [Related]
5. ATP1A3 mutation as a candidate cause of autosomal dominant cone-rod dystrophy. Zhou GH; Ma Y; Li ML; Zhou XY; Mou H; Jin ZB Hum Genet; 2020 Nov; 139(11):1391-1401. PubMed ID: 32440726 [TBL] [Abstract][Full Text] [Related]
6. Identification of a Novel Homozygous Nonsense Mutation Confirms the Implication of GNAT1 in Rod-Cone Dystrophy. Méjécase C; Laurent-Coriat C; Mayer C; Poch O; Mohand-Saïd S; Prévot C; Antonio A; Boyard F; Condroyer C; Michiels C; Blanchard S; Letexier M; Saraiva JP; Sahel JA; Audo I; Zeitz C PLoS One; 2016; 11(12):e0168271. PubMed ID: 27977773 [TBL] [Abstract][Full Text] [Related]
7. Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation. Lines MA; Hébert M; McTaggart KE; Flynn SJ; Tennant MT; MacDonald IM Ophthalmology; 2002 Oct; 109(10):1862-70. PubMed ID: 12359607 [TBL] [Abstract][Full Text] [Related]
8. Identification of Novel Mutations in the LRR-Cap Domain of C21orf2 in Japanese Patients With Retinitis Pigmentosa and Cone-Rod Dystrophy. Suga A; Mizota A; Kato M; Kuniyoshi K; Yoshitake K; Sultan W; Yamazaki M; Shimomura Y; Ikeo K; Tsunoda K; Iwata T Invest Ophthalmol Vis Sci; 2016 Aug; 57(10):4255-63. PubMed ID: 27548899 [TBL] [Abstract][Full Text] [Related]
9. Analysis of Early Cone Dysfunction in an In Vivo Model of Rod-Cone Dystrophy. Hassall MM; McClements ME; Barnard AR; Patricio MÍ; Aslam SA; Maclaren RE Int J Mol Sci; 2020 Aug; 21(17):. PubMed ID: 32842706 [TBL] [Abstract][Full Text] [Related]
10. GUCY2D Cone-Rod Dystrophy-6 Is a "Phototransduction Disease" Triggered by Abnormal Calcium Feedback on Retinal Membrane Guanylyl Cyclase 1. Sato S; Peshenko IV; Olshevskaya EV; Kefalov VJ; Dizhoor AM J Neurosci; 2018 Mar; 38(12):2990-3000. PubMed ID: 29440533 [TBL] [Abstract][Full Text] [Related]
14. Cone dystrophy with "supernormal" rod ERG: psychophysical testing shows comparable rod and cone temporal sensitivity losses with no gain in rod function. Stockman A; Henning GB; Michaelides M; Moore AT; Webster AR; Cammack J; Ripamonti C Invest Ophthalmol Vis Sci; 2014 Feb; 55(2):832-40. PubMed ID: 24370833 [TBL] [Abstract][Full Text] [Related]
15. Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy. Roosing S; Lamers IJ; de Vrieze E; van den Born LI; Lambertus S; Arts HH; ; Peters TA; Hoyng CB; Kremer H; Hetterschijt L; Letteboer SJ; van Wijk E; Roepman R; den Hollander AI; Cremers FP Am J Hum Genet; 2014 Aug; 95(2):131-42. PubMed ID: 25018096 [TBL] [Abstract][Full Text] [Related]
16. Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy. Hayashi T; Hosono K; Kurata K; Katagiri S; Mizobuchi K; Ueno S; Kondo M; Nakano T; Hotta Y Doc Ophthalmol; 2020 Apr; 140(2):147-157. PubMed ID: 31583501 [TBL] [Abstract][Full Text] [Related]