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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So far, Altmetric has seen 4 news stories from 4 outlets.

Taosheng Huang

Medical Health News, 14 May 2019

Jump to navigation Jump to search For other people named, see Taosheng Huang (disambiguation).

Mutations in SLC25A46 encoding a UGO1like protein cause an optic atrophy spectrum disorder

Bioportfolio, 14 Jul 2015

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

Researchers identify a novel disease gene causing neurodegenerative disorders

MedicalXpress, 13 Jul 2015

Researchers at the University of Miami (UM) have discovered and characterized a previously unknown disease gene linked to the…

New Gene Behind Neurodegenerative Disorders Discovered

Scicasts, 13 Jul 2015

Coral Gables, FL (Scicasts) - Researchers at the University of Miami (UM) have discovered and characterized a previously…

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