Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: NDUFA10[original query] |
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Abruptio placentae risk and genetic variations in mitochondrial biogenesis and oxidative phosphorylation: replication of a candidate gene association study. American journal of obstetrics and gynecology 2018 Sep . Workalemahu Tsegaselassie, Enquobahrie Daniel A, Gelaye Bizu, Thornton Timothy A, Tekola-Ayele Fasil, Sanchez Sixto E, Garcia Pedro J, Palomino Henry G, Hajat Anjum, Romero Roberto, Ananth Cande V, Williams Michelle |
Genetic variation and urine cadmium levels: ABCC1 effects in the Strong Heart Family Study. Environmental pollution (Barking, Essex : 1987) 2021 2 276 116717. Grau-Perez Maria, Voruganti V Saroja, Balakrishnan Poojitha, Haack Karin, Goessler Walter, Franceschini Nora, Redón Josep, Cole Shelley A, Navas-Acien Ana, Tellez-Plaza Mar |
Genotype and phenotype characteristics of West syndrome in 20 Vietnamese children: Two novel variants detected by next-generation sequencing. Epilepsy research 2023 1 190 107094. Duc Nguyen Minh, Thu Nguyen Thuy Minh, Bui Chi-Bao, Hoa Giang, Le Trung Hieu Nguy |
Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia. International journal of molecular sciences 2023 1 24 (2): . Kistol Denis, Tsygankova Polina, Krylova Tatiana, Bychkov Igor, Itkis Yulia, Nikolaeva Ekaterina, Mikhailova Svetlana, Sumina Maria, Pechatnikova Natalia, Kurbatov Sergey, Bostanova Fatima, Migiaev Ochir, Zakharova Ekateri |
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