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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Disease and ND4L[original query]
Mitochondrial genome mutations in 13 subunits of respiratory chain complexes in Chinese Han and Mongolian hypertensive individuals.
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis 2017 11 29 (7): 1090-1099.
Zhao Ying, Chen Xi, Li Haide, Zhu Chao, Li Yang, Liu Yu
Four novel mutations in the mitochondrial ND4 gene of complex I in patients with multiple sclerosis.
Biomedical reports 2019 12 11 (6): 257-268.
Alharbi Maram Atallah, Al-Kafaji Ghada, Khalaf Noureddine Ben, Messaoudi Safia Abdulsalam, Taha Safa, Daif Abdulqader, Bakhiet Mo
Association of mitochondrial variants and haplogroups identified by whole exome sequencing with Alzheimer's disease.
Alzheimer's & dementia : the journal of the Alzheimer's Association 2021 6 18 (2): 294-306.
Zhang Xiaoling, Farrell John J, Tong Tong, Hu Junming, Zhu Congcong, , Wang Li-San, Mayeux Richard, Haines Jonathan L, Pericak-Vance Margaret A, Schellenberg Gerard D, Lunetta Kathryn L, Farrer Lindsay
First mitochondrial genome-wide association study with metabolomics.
Human molecular genetics 2021 10 31 (19): 3367-3376.
Aboulmaouahib Brahim, Kastenmüller Gabi, Suhre Karsten, Zöllner Sebastian, Weissensteiner Hansi, Prehn Cornelia, Adamski Jerzy, Gieger Christian, Wang-Sattler Rui, Lichtner Peter, Strauch Konstantin, Flaquer Antòn
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