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

Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder have?

Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder has 207 citations in the OpenAlex counts ScholarIQ stores.

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

Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder has 2015 year in the ScholarIQ index.

What is the open-access status of Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder?

Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder has green oa status in the ScholarIQ index.

What is the DOI of Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder?

The DOI for Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder is on the source record.

What is the PMID of Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder?

The PMID for Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder is on the source record.

What is the OpenAlex record for Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder?

The OpenAlex for Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder is on the source record.