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Clinical and functional characterisation of the combined respiratory chain defect in two sisters due to autosomal recessive mutations in MTFMT
Neeve, Vivienne C.M., Pyle, Angela, Boczonadi, Veronika, Gomez-Duran, Aurora, Griffin, Helen, Santibanez-Koref, Mauro, Gaiser, Ulrike, Bauer, Peter, Tzschach, Andreas, Chinnery, Patrick F., Horvath, RVolume:
13
Language:
english
Journal:
Mitochondrion
DOI:
10.1016/j.mito.2013.03.002
Date:
November, 2013
File:
PDF, 487 KB
english, 2013