
Ion Campeanu
Pathology-Anatomic and Clinical Residency · Stony Brook Medicine
Credentials: · ·
History
- 2026–Present
- 2021–2025
Doctor of Medicine
Research
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder
Nature Genetics · 2015 · 176 citations
Scientific Reports · 2021 · Co-first of 9 authors · 48 citations
Insights into the genotype-phenotype correlation and molecular function of SLC25A46
Case report · Human Mutation · 2018 · 30 citations

1 paper · 1 as a resident

1 paper

1 paper
- CB
1 paper
- DW
1 paper

1 paper

1 paper

1 paper


