Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Mitochondrial Diseases and ND4[original query] |
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| Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss. Journal of human genetics 2010 Mar 55 (3): 147-54. Kato Tomofumi, Nishigaki Yutaka, Noguchi Yoshihiro, Ueno Hitomi, Hosoya Hiroko, Ito Taku, Kimura Yurika, Kitamura Ken, Tanaka Masas |
| Extensive screening system using suspension array technology to detect mitochondrial DNA point mutations. Mitochondrion 2010 Apr 10 (3): 300-8. Nishigaki Yutaka, Ueno Hitomi, Coku Jorida, Koga Yasutoshi, Fujii Tatsuya, Sahashi Ko, Nakano Kazutoshi, Yoneda Makoto, Nonaka Michiko, Tang Linya, Liou Chia-Wei, Paquis-Flucklinger Veronique, Harigaya Yasuo, Ibi Tohru, Goto Yu-ichi, Hosoya Hiroko, DiMauro Salvatore, Hirano Michio, Tanaka Masas |
| Leber's Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India. Investigative ophthalmology & visual science 2017 8 58 (10): 3923-3930. Khan Nahid Akhtar, Govindaraj Periyasamy, Soumittra Nagasamy, Sharma Sonika, Srilekha Sundaramoorthy, Ambika Selvakumar, Vanniarajan Ayyasamy, Meena Angamuthu Kanikannan, Uppin Megha S, Sundaram Challa, Bindu Parayil Sankaran, Gayathri Narayanappa, Taly Arun B, Thangaraj Kumarasa |
| NGS-based mtDNA Profiling Could Reveal Genetic Alterations in Schizophrenia. Current topics in medicinal chemistry 2021 6 21 (11): 938-948. Ivanova Elena Mihailova, Kandilarova Snezhina Mihailova, Lukanov Tzvetelin Ivanov, Naumova Elissaveta Jordanova, Akabalieva Katerina Valentinova, Milanova Vihra Krumo |
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