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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2013 | 1 |
2014 | 1 |
2021 | 1 |
2024 | 0 |
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A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus.
Commun Biol. 2021 Mar 1;4(1):266. doi: 10.1038/s42003-021-01784-0.
Commun Biol. 2021.
PMID: 33649486
Free PMC article.
Congenital hereditary endothelial dystrophy caused by SLC4A11 mutations progresses to Harboyan syndrome.
Siddiqui S, Zenteno JC, Rice A, Chacón-Camacho O, Naylor SG, Rivera-de la Parra D, Spokes DM, James N, Toomes C, Inglehearn CF, Ali M.
Siddiqui S, et al.
Cornea. 2014 Mar;33(3):247-51. doi: 10.1097/ICO.0000000000000041.
Cornea. 2014.
PMID: 24351571
Free PMC article.
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Mutational analysis of MIR184 in sporadic keratoconus and myopia.
Lechner J, Bae HA, Guduric-Fuchs J, Rice A, Govindarajan G, Siddiqui S, Abi Farraj L, Yip SP, Yap M, Das M, Souzeau E, Coster D, Mills RA, Lindsay R, Phillips T, Mitchell P, Ali M, Inglehearn CF, Sundaresan P, Craig JE, Simpson DA, Burdon KP, Willoughby CE.
Lechner J, et al.
Invest Ophthalmol Vis Sci. 2013 Aug 5;54(8):5266-72. doi: 10.1167/iovs.13-12035.
Invest Ophthalmol Vis Sci. 2013.
PMID: 23833072
Free article.
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