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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: Dec 5, 2023. (Total: 223688Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Mitochondrial Complex V Deficiency[original query]
Mitochondrial DNA polymorphisms and haplogroups in Parkinson's disease and control individuals with a similar genetic background.
Journal of human genetics 2008 53 (4): 349-56.
Latsoudis Helen, Spanaki Cleanthe, Chlouverakis Grigoris, Plaitakis Andre
Neuronal complex I deficiency occurs throughout the Parkinson's disease brain, but is not associated with neurodegeneration or mitochondrial DNA damage.
Acta neuropathologica 2017 12 135 (3): 409-425.
Flønes Irene H, Fernandez-Vizarra Erika, Lykouri Maria, Brakedal Brage, Skeie Geir Olve, Miletic Hrvoje, Lilleng Peer K, Alves Guido, Tysnes Ole-Bjørn, Haugarvoll Kristoffer, Dölle Christian, Zeviani Massimo, Tzoulis Charalamp
Impact of a NDUFC2 Variant on the Occurrence of Acute Coronary Syndromes.
Frontiers in cardiovascular medicine 2022 6 9 921244.
Gallo Giovanna, Migliarino Serena, Cotugno Maria, Stanzione Rosita, Burocchi Simone, Bianchi Franca, Marchitti Simona, Autore Camillo, Volpe Massimo, Rubattu Speran
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