Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: SCO2[original query] |
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Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies. JAMA 2014 Jul 312 (1): 68-77. Taylor Robert W, Pyle Angela, Griffin Helen, Blakely Emma L, Duff Jennifer, He Langping, Smertenko Tania, Alston Charlotte L, Neeve Vivienne C, Best Andrew, Yarham John W, Kirschner Janbernd, Schara Ulrike, Talim Beril, Topaloglu Haluk, Baric Ivo, Holinski-Feder Elke, Abicht Angela, Czermin Birgit, Kleinle Stephanie, Morris Andrew A M, Vassallo Grace, Gorman Grainne S, Ramesh Venkateswaran, Turnbull Douglass M, Santibanez-Koref Mauro, McFarland Robert, Horvath Rita, Chinnery Patrick |
ADRB2 gly16gly Genotype, Cardiac Output, and Cerebral Oxygenation in Patients Undergoing Anesthesia for Abdominal Aortic Aneurysm Surgery. Anesthesia and analgesia 2016 Sep . Staalsø Jonatan Myrup, Rokamp Kim Zillo, Olesen Niels D, Lonn Lars, Secher Niels H, Olsen Niels V, Mantoni Teit, Helgstrand Ulf, Nielsen Henning |
Association between SCO2 mutation and extreme myopia in Japanese patients. Japanese journal of ophthalmology 2016 Jul 60 (4): 319-25. Wakazono Tomotaka, Miyake Masahiro, Yamashiro Kenji, Yoshikawa Munemitsu, Yoshimura Nagahi |
Genetic alterations in fatty acid transport and metabolism genes are associated with metastatic progression and poor prognosis of human cancers. Scientific reports 2016 6 18669. Nath Aritro, Chan Christi |
Expanding the Phenotypic and Genotypic Landscape of Nonsyndromic High Myopia: A Cross-Sectional Study in 731 Chinese Patients. Investigative ophthalmology & visual science 2019 9 60 (12): 4052-4062. Cai Xue-Bi, Zheng Yi-Han, Chen De-Fu, Zhou Fang-Yue, Xia Lu-Qi, Wen Xin-Ran, Yuan Yi-Min, Han Fang, Piao Shun-Yu, Zhuang Wenjuan, Lu Fan, Qu Jia, Yu A-Yong, Jin Zi-Bi |
Mutational screening of AGRN, SLC39A5, SCO2, P4HA2, BSG, ZNF644, and CPSF1 in a Chinese cohort of 103 patients with nonsyndromic high myopia. Molecular vision 2022 1 27 706-717. Zheng Yi-Han, Cai Xue-Bi, Xia Lu-Qi, Zhou Fang-Yue, Wen Xin-Ran, Chen De-Fu, Han Fang, Zhou Kai-Jing, Jin Zi-Bing, Zhuang Wen-Juan, Lin Bi |
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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- Page last updated:Apr 22, 2024
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