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Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits. [electronic resource] by
- Glasgow, Ruth I C
- Thompson, Kyle
- Barbosa, Inês A
- He, Langping
- Alston, Charlotte L
- Deshpande, Charu
- Simpson, Michael A
- Morris, Andrew A M
- Neu, Axel
- Löbel, Ulrike
- Hall, Julie
- Prokisch, Holger
- Haack, Tobias B
- Hempel, Maja
- McFarland, Robert
- Taylor, Robert W
Producer: 20180802
In:
Neurogenetics vol. 18
Availability: No items available.
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