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Novel membrane frizzled-related protein gene mutation as cause of posterior microphthalmia resulting in high hyperopia with macular folds.
Acta Ophthalmol. 2014 May;92(3):276-81. doi: 10.1111/aos.12105. Epub 2013 Jun 7.
Acta Ophthalmol. 2014.
PMID: 23742260
Free PMC article.
Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy.
de Muijnck C, Haer-Wigman L, van Everdingen JAM, Lushchyk T, Heutinck PAT, van Dooren MF, Kievit AJA, Verhoeven VJM, Simon MEH, Wasmann RA, Notting IC, De Baere E, Walraedt S, De Zaeytijd J, Van den Broeck F, Leroy BP, Boon CJF, van Genderen MM.
de Muijnck C, et al. Among authors: wasmann ra.
Sci Rep. 2024 Oct 3;14(1):22956. doi: 10.1038/s41598-024-74364-x.
Sci Rep. 2024.
PMID: 39363032
Free PMC article.
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