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mtDNA/nDNA ratio in 14484 LHON mitochondrial mutation carriers.
Nishioka, Tomoki; Soemantri, Augustinus; Ishida, Takafumi.
Affiliation
  • Nishioka T; Human Biology and Genetics, Department of Biological Sciences, Graduate School of Science, University of Tokyo, Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.
  • Soemantri A; Faculty of Medicine, Diponegoro University, Semarang, Indonesia.
  • Ishida T; Human Biology and Genetics, Department of Biological Sciences, Graduate School of Science, University of Tokyo, Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan. tishida@biol.s.u-tokyo.ac.jp.
J Hum Genet ; 49(12): 701-705, 2004.
Article in En | MEDLINE | ID: mdl-15635488

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Optic Atrophy, Hereditary, Leber / Heterozygote / Mutation Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: J Hum Genet Journal subject: GENETICA MEDICA Year: 2004 Document type: Article Affiliation country: Japan Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Optic Atrophy, Hereditary, Leber / Heterozygote / Mutation Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: J Hum Genet Journal subject: GENETICA MEDICA Year: 2004 Document type: Article Affiliation country: Japan Country of publication: United kingdom