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

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Description scientific journal article
Author/s

author: Carlos E Prada  Alessandra Maresca  Leonardo Caporali  Valerio Carelli  Omar A Abdul-Rahman  Raffaele Lodi  Rocco Liguori  Robert B Hufnagel  Chiara La Morgia  Taosheng Huang 

Publication date August 1, 2015
Language English
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