Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder - Concepedia

Concepedia

Publication | Open Access

Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder

DOI Full Paper Access

200

Citations

33

References

2015

Year

Alexander J. Abrams, Robert B. Hufnagel, Adriana Rebelo, Claudia Zanna, Neville Patel, Michael Gonzalez, Ion John Campeanu, Laurie B. Griffin, Saskia Groenewald, Alleene V. Strickland,

Nature Genetics

Somatic VariantMendelian DisorderGenetic DisorderGeneticsMolecular BiologyMolecular GeneticsDisease Gene IdentificationProtein GeneticsMedicineUgo1-like Protein

References

	Year	Citations

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