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Author/Creator Rodenburg, Richard J.T.

1. Mutations in COA6 cause Cytochrome c Oxidase Deficiency and Neonatal Hypertrophic Cardiomyopathy. Issue 1 (18th November 2014)

Authors:
Baertling, Fabian; A.M. van den Brand, Mariel; Hertecant, Jozef L.; Al‐Shamsi, Aisha; P. van den Heuvel, Lambert; Distelmaier, Felix; Mayatepek, Ertan; Smeitink, Jan A.; Nijtmans, Leo G.J.; Rodenburg, Richard J.T.
Journal:
Human mutation
Issue:
Volume 36:Issue 1(2015:Jan.)
Page Start:
34
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Variants in Mitochondrial ATP Synthase Cause Variable Neurologic Phenotypes. Issue 2 (20th January 2022)

Authors:
Zech, Michael; Kopajtich, Robert; Steinbrücker, Katja; Bris, Céline; Gueguen, Naig; Feichtinger, René G.; Achleitner, Melanie T.; Duzkale, Neslihan; Périvier, Maximilien; Koch, Johannes; Engelhardt, Harald; Freisinger, Peter; Wagner, Matias; Brunet, Theresa; Berutti, Riccardo; Smirnov, Dmitrii; N...
Journal:
Annals of neurology
Issue:
Volume 91:Issue 2(2022)
Page Start:
225
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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