Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits

Por 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.
Publicado no Neurogenetics (2017)