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Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder
PaperCitations, authors & open-access status
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 207 citations, 2015 year and green oa status.
207
Citations
2015
Year
green
OA Status