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Fabian Baertling

Showing results (21-30 of 24) with videos related to

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Human Mutation|October 24, 2014
Mutations in COA6 cause cytochrome c oxidase deficiency and neonatal hypertrophic cardiomyopathyFabian Baertling, Mariel A M van den Brand, Jozef L Hertecant, et al.
Biochimica Et Biophysica Acta. Bioenergetics|April 11, 2020
TMEM70 functions in the assembly of complexes I and VLaura Sánchez-Caballero, Dei M Elurbe, Fabian Baertling, et al.
Brain : a Journal of Neurology|December 3, 2015
Human thioredoxin 2 deficiency impairs mitochondrial redox homeostasis and causes early-onset neurodegenerationEliska Holzerova, Katharina Danhauser, Tobias B Haack, et al.
Journal of Medical Genetics|October 17, 2021
Human COQ4 deficiency: delineating the clinical, metabolic and neuroimaging phenotypesLucia Laugwitz, Annette Seibt, Diran Herebian, et al.
Pageof 3

Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
Human Mutation|October 24, 2014
Mutations in COA6 cause cytochrome c oxidase deficiency and neonatal hypertrophic cardiomyopathyFabian Baertling, Mariel A M van den Brand, Jozef L Hertecant, et al.
Biochimica Et Biophysica Acta. Bioenergetics|April 11, 2020
TMEM70 functions in the assembly of complexes I and VLaura Sánchez-Caballero, Dei M Elurbe, Fabian Baertling, et al.
Brain : a Journal of Neurology|December 3, 2015
Human thioredoxin 2 deficiency impairs mitochondrial redox homeostasis and causes early-onset neurodegenerationEliska Holzerova, Katharina Danhauser, Tobias B Haack, et al.
Journal of Medical Genetics|October 17, 2021
Human COQ4 deficiency: delineating the clinical, metabolic and neuroimaging phenotypesLucia Laugwitz, Annette Seibt, Diran Herebian, et al.
Pageof 3