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Journal Abstract Search

228 related items for PubMed ID: 33302512

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  • 3. Novel Missense Mutations in BEST1 Are Associated with Bestrophinopathies in Lebanese Patients.
    Jaffal L, Joumaa WH, Assi A, Helou C, Condroyer C, El Dor M, Cherfan G, Zeitz C, Audo I, Zibara K, El Shamieh S.
    Genes (Basel); 2019 Feb 18; 10(2):. PubMed ID: 30781664
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  • 4. Screening for BEST1 gene mutations in Chinese patients with bestrophinopathy.
    Tian R, Yang G, Wang J, Chen Y.
    Mol Vis; 2014 Feb 18; 20():1594-604. PubMed ID: 25489231
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  • 5. Detailed analysis of family with autosomal recessive bestrophinopathy associated with new BEST1 mutation.
    Kubota D, Gocho K, Akeo K, Kikuchi S, Sugahara M, Matsumoto CS, Shinoda K, Mizota A, Yamaki K, Takahashi H, Kameya S.
    Doc Ophthalmol; 2016 Jun 18; 132(3):233-43. PubMed ID: 27071392
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  • 10. Multimodal imaging and genetic characteristics of autosomal recessive bestrophinopathy.
    Tekin K, Dulger SC, Horozoglu Ceran T, Inanc M, Ozdal PC, Teke MY.
    J Fr Ophtalmol; 2024 Jun 18; 47(6):104097. PubMed ID: 38518704
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  • 15. The Retinal Phenotype Associated with the p.Pro101Thr BEST1 Variant.
    Bianco L, Arrigo A, Antropoli A, Del Fabbro S, Mauro L, Pina A, Bandello F, Battaglia Parodi M.
    Ophthalmol Retina; 2024 Mar 18; 8(3):288-297. PubMed ID: 37717827
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  • 17. Clinical and genetic features in autosomal recessive bestrophinopathy in Chinese cohort.
    Zhao D, Gu VY, Wang Y, Peng J, Lyu J, Fei P, Xu Y, Zhang X, Zhao P.
    BMC Ophthalmol; 2024 Jul 24; 24(1):308. PubMed ID: 39048936
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  • 20. Non-vasogenic cystoid maculopathy in autosomal recessive bestrophinopathy: novel insights from NIR-FAF and OCTA imaging.
    Bianco L, Arrigo A, Antropoli A, Saladino A, Aragona E, Bandello F, Parodi MB.
    Ophthalmic Genet; 2024 Feb 24; 45(1):44-50. PubMed ID: 37041716
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