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A T M Hendrickx

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Neuromuscular Disorders : NMD|September 8, 2004
Increased risk for cardiorespiratory failure associated with the A3302G mutation in the mitochondrial DNA encoded tRNALeu(UUR) geneB J C van den Bosch, I F M de Coo, A T M Hendrickx, et al.
Human Reproduction Update|March 30, 2012
PGD and heteroplasmic mitochondrial DNA point mutations: a systematic review estimating the chance of healthy offspringD M E I Hellebrekers, R Wolfe, A T M Hendrickx, et al.
Mitochondrion|June 8, 2011
Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European populationS Bonneux, E Fransen, E Van Eyken, et al.
Journal of Medical Genetics|June 23, 2009
Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndromeM Gerards, W Sluiter, B J C van den Bosch, et al.
JIMD Reports|March 4, 2015
Two Novel Mutations in the SLC25A4 Gene in a Patient with Mitochondrial MyopathyI M L W Körver-Keularts, M de Visser, H D Bakker, et al.
Pageof 1

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

Sort By:
Pageof 1
Neuromuscular Disorders : NMD|September 8, 2004
Increased risk for cardiorespiratory failure associated with the A3302G mutation in the mitochondrial DNA encoded tRNALeu(UUR) geneB J C van den Bosch, I F M de Coo, A T M Hendrickx, et al.
Human Reproduction Update|March 30, 2012
PGD and heteroplasmic mitochondrial DNA point mutations: a systematic review estimating the chance of healthy offspringD M E I Hellebrekers, R Wolfe, A T M Hendrickx, et al.
Mitochondrion|June 8, 2011
Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European populationS Bonneux, E Fransen, E Van Eyken, et al.
Journal of Medical Genetics|June 23, 2009
Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndromeM Gerards, W Sluiter, B J C van den Bosch, et al.
JIMD Reports|March 4, 2015
Two Novel Mutations in the SLC25A4 Gene in a Patient with Mitochondrial MyopathyI M L W Körver-Keularts, M de Visser, H D Bakker, et al.
Pageof 1