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Genet Couns
; 26(2): 259-62, 2015.
Article
in English
| MEDLINE
| ID: mdl-26349199
Subject(s)
Ataxia/genetics , Electron-Transferring Flavoproteins/genetics , Iron-Sulfur Proteins/genetics , Mitochondrial Diseases/genetics , Muscle Weakness/genetics , Oxidoreductases Acting on CH-NH Group Donors/genetics , Ubiquinone/deficiency , Adult , Humans , Male , Mutation , Ubiquinone/genetics , Young Adult
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