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

Glasgow, Ruth I. C.; Thompson, Kyle; Barbosa, Ines A.; He, Langping; Alston, Charlotte L.; Deshpande, Charu; Simpson, Michael A.; Morris, Andrew A. M.; Neu, Axel; Loebel, Ulrike; Hall, Julie; Prokisch, Holger; Haack, Tobias B.; Hempel, Maja; McFarland, Robert; Taylor, Robert W.

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

Author:

Glasgow, Ruth I. C.; Thompson, Kyle; Barbosa, Ines A.; He, Langping; Alston, Charlotte L.; Deshpande, Charu; Simpson, Michael A.; Morris, Andrew A. M.; Neu, Axel; Loebel, Ulrike; Hall, Julie; Prokisch, Holger; Haack, Tobias B.; Hempel, Maja; McFarland, Robert; Taylor, Robert W.

Tübinger Autor(en):

Haack, Tobias

Published in:

Neurogenetics (2017), Bd. 18, H. 4, S. 227-235

Verlagsangabe:

Springer

Language:

English

Full text:

http://dx.doi.org/10.1007/s10048-017-0526-4

ISSN:

1364-6753