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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1977 1
1992 2
1993 2
1998 2
2000 1
2003 1
2020 1
2023 4
2024 2

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PubMed for id: 1676440554

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Page 1
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. Bianco L, et al. Ophthalmol Retina. 2024 Mar;8(3):288-297. doi: 10.1016/j.oret.2023.09.012. Epub 2023 Sep 16. Ophthalmol Retina. 2024. PMID: 37717827
Nonsyndromic Retinitis Pigmentosa Overview.
Fahim AT, Daiger SP, Weleber RG. Fahim AT, et al. 2000 Aug 4 [updated 2023 Apr 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2000 Aug 4 [updated 2023 Apr 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301590 Free Books & Documents. Review.
Bestrophinopathies.
MacDonald IM, Lee T, Lawrence J. MacDonald IM, et al. 2003 Sep 30 [updated 2020 Jul 16]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2003 Sep 30 [updated 2020 Jul 16]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301346 Free Books & Documents. Review.
Identification of the gene responsible for Best macular dystrophy.
Petrukhin K, Koisti MJ, Bakall B, Li W, Xie G, Marknell T, Sandgren O, Forsman K, Holmgren G, Andreasson S, Vujic M, Bergen AA, McGarty-Dugan V, Figueroa D, Austin CP, Metzker ML, Caskey CT, Wadelius C. Petrukhin K, et al. Nat Genet. 1998 Jul;19(3):241-7. doi: 10.1038/915. Nat Genet. 1998. PMID: 9662395