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.
3. A TULP1 founder mutation, p.Gln301*, underlies a recognisable congenital rod-cone dystrophy phenotype on the Arabian Peninsula. Khan AO; Bergmann C; Eisenberger T; Bolz HJ Br J Ophthalmol; 2015 Apr; 99(4):488-92. PubMed ID: 25342276 [TBL] [Abstract][Full Text] [Related]
4. The phenotype of Severe Early Childhood Onset Retinal Dystrophy (SECORD) from mutation of RPE65 and differentiation from Leber congenital amaurosis. Weleber RG; Michaelides M; Trzupek KM; Stover NB; Stone EM Invest Ophthalmol Vis Sci; 2011 Jan; 52(1):292-302. PubMed ID: 20811047 [TBL] [Abstract][Full Text] [Related]
5. 'Cone dystrophy with supranormal rod response' in children. Khan AO; Alrashed M; Alkuraya FS Br J Ophthalmol; 2012 Mar; 96(3):422-6. PubMed ID: 21900228 [TBL] [Abstract][Full Text] [Related]
6. Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations. Mackay DS; Ocaka LA; Borman AD; Sergouniotis PI; Henderson RH; Moradi P; Robson AG; Thompson DA; Webster AR; Moore AT Invest Ophthalmol Vis Sci; 2011 May; 52(6):3032-8. PubMed ID: 21310915 [TBL] [Abstract][Full Text] [Related]
7. Clinical, Ophthalmic, and Genetic Characterization of RPGRIP1-Associated Leber Congenital Amaurosis/Early-Onset Severe Retinal Dystrophy. Daich Varela M; Jeste M; de Guimaraes TAC; Mahroo OA; Arno G; Webster AR; Michaelides M Am J Ophthalmol; 2024 Oct; 266():255-263. PubMed ID: 38768745 [TBL] [Abstract][Full Text] [Related]
8. Peripherin mutations cause a distinct form of recessive Leber congenital amaurosis and dominant phenotypes in asymptomatic parents heterozygous for the mutation. Khan AO; Al Rashaed S; Neuhaus C; Bergmann C; Bolz HJ Br J Ophthalmol; 2016 Feb; 100(2):209-15. PubMed ID: 26061163 [TBL] [Abstract][Full Text] [Related]
13. Clinical characteristics of rod and cone photoreceptor dystrophies in patients with mutations in the C8orf37 gene. van Huet RA; Estrada-Cuzcano A; Banin E; Rotenstreich Y; Hipp S; Kohl S; Hoyng CB; den Hollander AI; Collin RW; Klevering BJ Invest Ophthalmol Vis Sci; 2013 Jul; 54(7):4683-90. PubMed ID: 23788369 [TBL] [Abstract][Full Text] [Related]
14. Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1. Henderson RH; Mackay DS; Li Z; Moradi P; Sergouniotis P; Russell-Eggitt I; Thompson DA; Robson AG; Holder GE; Webster AR; Moore AT Br J Ophthalmol; 2011 Jun; 95(6):811-7. PubMed ID: 20956273 [TBL] [Abstract][Full Text] [Related]
15. Identification of mutations in the AIPL1, CRB1, GUCY2D, RPE65, and RPGRIP1 genes in patients with juvenile retinitis pigmentosa. Booij JC; Florijn RJ; ten Brink JB; Loves W; Meire F; van Schooneveld MJ; de Jong PT; Bergen AA J Med Genet; 2005 Nov; 42(11):e67. PubMed ID: 16272259 [TBL] [Abstract][Full Text] [Related]
17. The ophthalmic phenotype of IFT140-related ciliopathy ranges from isolated to syndromic congenital retinal dystrophy. Bifari IN; Elkhamary SM; Bolz HJ; Khan AO Br J Ophthalmol; 2016 Jun; 100(6):829-33. PubMed ID: 26359340 [TBL] [Abstract][Full Text] [Related]
18. Biallelic Huckfeldt RM; Grigorian F; Place E; Comander JI; Vavvas D; Young LH; Yang P; Shurygina M; Pierce EA; Pennesi ME Mol Vis; 2020; 26():423-433. PubMed ID: 32565670 [TBL] [Abstract][Full Text] [Related]
19. Early-onset severe rod-cone dystrophy in young children with RPE65 mutations. Lorenz B; Gyürüs P; Preising M; Bremser D; Gu S; Andrassi M; Gerth C; Gal A Invest Ophthalmol Vis Sci; 2000 Aug; 41(9):2735-42. PubMed ID: 10937591 [TBL] [Abstract][Full Text] [Related]