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A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions
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Journal Title: | Frontiers in Genetics |
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Authors and Corporations: | , , , , , , |
In: | Frontiers in Genetics, 5, 2014 |
Type of Resource: | E-Article |
Language: | Undetermined |
published: |
Frontiers Media SA
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Subjects: |