Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Hearing and POLG[original query] |
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Peripheral neuropathy predicts nuclear gene defect in patients with mitochondrial ophthalmoplegia. Brain : a journal of neurology 2014 Dec 137 (Pt 12): 3200-12. Horga Alejandro, Pitceathly Robert D S, Blake Julian C, Woodward Catherine E, Zapater Pedro, Fratter Carl, Mudanohwo Ese E, Plant Gordon T, Houlden Henry, Sweeney Mary G, Hanna Michael G, Reilly Mary |
Increased burden of mitochondrial DNA deletions and point mutations in early-onset age-related hearing loss in mitochondrial mutator mice. Experimental gerontology 2019 7 125 110675. Kim Mi-Jung, Haroon Suraiya, Chen Guang-Di, Ding Dalian, Wanagat Jonathan, Liu Lijie, Zhang Yanping, White Karessa, Park Hyo-Jin, Han Chul, Boyd Kevin, Caicedo Isabela, Evans Kaitlyn, Linser Paul J, Tanokura Masaru, Prolla Tomas, Salvi Richard, Vermulst Marc, Someya Shinic |
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome. Journal of neurology 2021 1 268 (6): 2192-2207. Chakrabarty Sanjiban, Govindaraj Periyasamy, Sankaran Bindu Parayil, Nagappa Madhu, Kabekkodu Shama Prasada, Jayaram Pradyumna, Mallya Sandeep, Deepha Sekar, Ponmalar J N Jessiena, Arivinda Hanumanthapura R, Meena Angamuthu Kanikannan, Jha Rajan Kumar, Sinha Sanjib, Gayathri Narayanappa, Taly Arun B, Thangaraj Kumarasamy, Satyamoorthy Kapaet |
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