Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Hearing 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 |
A novel m.11406 T > A mutation in mitochondrial ND4 gene causes MELAS syndrome. Mitochondrion 2020 7 54 57-64. Lin Yan, Xu Xuebi, Zhao Dandan, Liu Fuchen, Luo Yuebei, Du Jixiang, Wang Dongdong, Ji Kunqian, Zhao Yuying, Yan Chuanz |
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