CHCHD2 accumulates in distressed mitochondria and facilitates oligomerization of CHCHD10.

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第一作者： Xiaoping,Huang

第一单位： Inherited Movement Disorders Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

作者： Xiaoping,Huang ^[1] ; Beverly P,Wu ^[1] ; Diana,Nguyen ^[1] ; Yi-Ting,Liu ^[1] ; Melika,Marani ^[1] ; Jürgen,Hench ^[2] ; Paule,Bénit ^[3] ; Vera,Kozjak-Pavlovic ^[4] ; Pierre,Rustin ^[3] ; Stephan,Frank ^[5] ; Derek P,Narendra ^[2]

作者单位： Inherited Movement Disorders Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA. ^[1] Division of Neuropathology, Institute of Pathology, University Hospital Basel, Basel, Switzerland. ^[2] INSERM UMR 1141, Hôpital Robert Debré, Paris, France. ^[3] Department of Microbiology, Biocenter, University of Wuerzburg, Am Hubland, Wuerzburg, Germany. ^[4] Université Paris Diderot, Paris, France. ^[5]

DOI 10.1093/hmg/ddy340

PMID 30285108

发布时间 2019-11-20

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Human molecular genetics

2019年28卷2期

349页

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CHCHD2 accumulates in distressed mitochondria and facilitates oligomerization of CHCHD10.

Human molecular genetics

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Human molecular genetics

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CHCHD2 accumulates in distressed mitochondria and facilitates oligomerization of CHCHD10.

Human molecular genetics

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Human molecular genetics

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