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Query Trace: Mitochondrial Diseases and RNR1[orginal query]

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 Similar articles in PubMed
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 Similar articles in PubMed
[Prevalence of the A1555G MTDNA mutation in sporadic hearing-impaired patients without known history of aminoglycoside treatment]. Acta otorrinolaringológica española 0 62 (2): 83-6. Morales Angulo Carmelo, Gallo-Terán Jaime, Señaris Blanca, Fontalva Ana, González-Aguado Rocío, Fernández-Luna José Lu Similar articles in PubMed
Sequence variations of mitochondrial DNA and individual sensitivity to the ototoxic effect of cisplatin. Anticancer research 0 23 (2B): 1249-55. Peters Ulrike, Preisler-Adams S, Lanvers-Kaminsky Claudia, Jürgens Heribert, Lamprecht-Dinnesen Antoinet Similar articles in PubMed