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Mutations in NSUN3, a Mitochondrial Methyl Transferase Gene, Cause Inherited Optic Neuropathy.
Genes (Basel). 2024 Apr 24;15(5):530. doi: 10.3390/genes15050530.
Genes (Basel). 2024.
PMID: 38790159
Free PMC article.
Delineating Wolfram-like syndrome: A systematic review and discussion of the WFS1-associated disease spectrum.
de Muijnck C, Brink JBT, Bergen AA, Boon CJF, van Genderen MM.
de Muijnck C, et al. Among authors: brink jbt.
Surv Ophthalmol. 2023 Jul-Aug;68(4):641-654. doi: 10.1016/j.survophthal.2023.01.012. Epub 2023 Feb 9.
Surv Ophthalmol. 2023.
PMID: 36764396
Free article.
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