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Bertil Macao

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

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Movement Disorders : Official Journal of the Movement Disorder Society|July 6, 2022
TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective StudyMarco Percetti, Giulia Franco, Edoardo Monfrini, et al.
Science Advances|July 3, 2021
The mitochondrial single-stranded DNA binding protein is essential for initiation of mtDNA replicationMin Jiang, Xie Xie, Xuefeng Zhu, et al.
Nature|April 9, 2025
Small molecules restore mutant mitochondrial DNA polymerase activitySebastian Valenzuela, Xuefeng Zhu, Bertil Macao, et al.
The Journal of Clinical Investigation|September 25, 2019
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorderValentina Del Dotto, Farid Ullah, Ivano Di Meo, 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.
Movement Disorders : Official Journal of the Movement Disorder Society|July 6, 2022
TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective StudyMarco Percetti, Giulia Franco, Edoardo Monfrini, et al.
Science Advances|July 3, 2021
The mitochondrial single-stranded DNA binding protein is essential for initiation of mtDNA replicationMin Jiang, Xie Xie, Xuefeng Zhu, et al.
Nature|April 9, 2025
Small molecules restore mutant mitochondrial DNA polymerase activitySebastian Valenzuela, Xuefeng Zhu, Bertil Macao, et al.
The Journal of Clinical Investigation|September 25, 2019
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorderValentina Del Dotto, Farid Ullah, Ivano Di Meo, et al.
Pageof 3