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Pathogenic mutations of nuclear genes associated with mitochondrial disorders.

• Authors : Zhu X; College of Life Science, Zhejiang University, Hangzhou 310058, Peopleos Republic of China.; Peng X

Subjects: Genes* ; Mutation*; Cell Nucleus/Cell Nucleus/Cell Nucleus/*genetics

• Source: Acta biochimica et biophysica Sinica [Acta Biochim Biophys Sin (Shanghai)] 2009 Mar; Vol. 41 (3), pp. 179-87.Publisher: China Science Publishing & Media Ltd Country of Publication: China NLM ID: 101206716 Publication Model: Print Cited Medium: Internet ISSN:

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Agricola

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MmisAT and MmisP: an efficient and accurate suite of variant analysis toolkit for primary mitochondrial diseases

• Authors : Huang, Shuangshuang; Wu, Zhaoyu; Wang, Tong

• Source: Human Genomics. November 27, 2023, Vol. 17 Issue 1

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The molecular basis of human complex I deficiency.

• Authors : Tucker EJ; Murdoch Childrens Research Institute, Royal Children's Hospital, Melbourne, Australia. ; Compton AG

Subjects: Electron Transport Complex I/Electron Transport Complex I/Electron Transport Complex I/*deficiency ; Genes/Genes/Genes/*genetics ; Metabolism, Inborn Errors/Metabolism, Inborn Errors/Metabolism, Inborn Errors/*genetics

• Source: IUBMB life [IUBMB Life] 2011 Sep; Vol. 63 (9), pp. 669-77. Date of Electronic Publication: 2011 Jul 15.Publisher: Published for the International Union of Biochemistry and Molecular Biology by Taylor & Francis Country of Publication: England NLM ID: 100888706

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Agricola

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Agricola

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Multisystem mitochondrial diseases due to mutations in mtDNA-encoded subunits of complex I

• Authors : Danhelovska, Tereza; Kolarova, Hana; Zeman, Jiri

• Source: BMC Pediatrics. January 29, 2020, Vol. 20 Issue 1

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Agricola

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Research from Department of Obstetrics and Gynecology in the Area of Science Published (The mining and construction of a knowledge base for gene-disease association in mitochondrial diseases)

• Source: Obesity, Fitness & Wellness Week. January 8, 2022, 3432

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