G H. Renkema
Nijmegen, GE 6500HB, Netherlands
Last Updated: 09/26/2026
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Found 9 publications
Stimulation of cholesterol biosynthesis in mitochondrial complex I-deficiency lowers reductive stress and improves motor function and survival in mice.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: August 27, 2020
A Drosophila Mitochondrial Complex I Deficiency Phenotype Array.
Journal: Frontiers in genetics
Published: August 03, 2018
Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions.
Journal: Human genetics
Published: February 02, 2017
Mutations in SELENBP1, encoding a novel human methanethiol oxidase, cause extraoral halitosis.
Journal: Nature genetics
Published: December 21, 2016
Statin-Induced Myopathy Is Associated with Mitochondrial Complex III Inhibition.
Journal: Cell metabolism
Published: January 14, 2015
CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder.
Journal: American journal of human genetics
Published: November 17, 2014
SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors.
Journal: European journal of human genetics : EJHG
Published: August 26, 2013
A complex V ATP5A1 defect causes fatal neonatal mitochondrial encephalopathy.
Journal: Brain : a journal of neurology
Published: April 20, 2013
Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness.
Journal: Nature genetics
Published: March 01, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026