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

Overview of attention for article published in Nature Genetics, July 2015

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Neuroscience Library/Bibliothèque des Neurosciences, 28 Jul 2015

Researchers Identify a Novel Disease Gene Causing Neurodegenerative…

Neurogenetica Clinica Pisa, 24 Jul 2015

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

Bioenergetyka, 15 Jul 2015

Stephan Zuchner, Taosheng Huang and colleagues show that recessive mutations in SLC25A46 cause optic atrophy with additional…

Cancer Metabolism, 15 Jul 2015

very nice work!!

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