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Saskia J G Hoefs

Showing results (1-10 of 5) with videos related to

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Mitochondrion|July 24, 2012
Molecular base of biochemical complex I deficiencySaskia J G Hoefs, Richard J Rodenburg, Jan A M Smeitink, et al.
European Journal of Human Genetics : EJHG|December 15, 2010
NDUFA10 mutations cause complex I deficiency in a patient with Leigh diseaseSaskia J G Hoefs, Francjan J van Spronsen, Ellen W H Lenssen, et al.
Human Mutation|April 23, 2009
Baculovirus complementation restores a novel NDUFAF2 mutation causing complex I deficiencySaskia J G Hoefs, Cindy E J Dieteren, Richard J Rodenburg, et al.
Molecular Genetics and Metabolism|April 13, 2010
Novel mutations in the NDUFS1 gene cause low residual activities in human complex I deficienciesSaskia J G Hoefs, Ola H Skjeldal, Richard J Rodenburg, et al.
American Journal of Human Genetics|June 3, 2008
NDUFA2 complex I mutation leads to Leigh diseaseSaskia J G Hoefs, Cindy E J Dieteren, Felix Distelmaier, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Mitochondrion|July 24, 2012
Molecular base of biochemical complex I deficiencySaskia J G Hoefs, Richard J Rodenburg, Jan A M Smeitink, et al.
European Journal of Human Genetics : EJHG|December 15, 2010
NDUFA10 mutations cause complex I deficiency in a patient with Leigh diseaseSaskia J G Hoefs, Francjan J van Spronsen, Ellen W H Lenssen, et al.
Human Mutation|April 23, 2009
Baculovirus complementation restores a novel NDUFAF2 mutation causing complex I deficiencySaskia J G Hoefs, Cindy E J Dieteren, Richard J Rodenburg, et al.
Molecular Genetics and Metabolism|April 13, 2010
Novel mutations in the NDUFS1 gene cause low residual activities in human complex I deficienciesSaskia J G Hoefs, Ola H Skjeldal, Richard J Rodenburg, et al.
American Journal of Human Genetics|June 3, 2008
NDUFA2 complex I mutation leads to Leigh diseaseSaskia J G Hoefs, Cindy E J Dieteren, Felix Distelmaier, et al.
Pageof 1