Prevalence of Japanese dialysis patients with an A-to-G mutation at nucleotide 3243 of the mitochondrial tRNALeu(UUR) gene-Reference-Cited by-同舟云学术

Prevalence of Japanese dialysis patients with an A-to-G mutation at nucleotide 3243 of the mitochondrial tRNALeu(UUR) gene

Published:2000-03-01 Issue:3 Volume:15 Page:385-388
ISSN:1460-2385
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:

Author:

Yamagata Kunihiro,Tomida Chie,Umeyama Kazuiro,Urakami Ken-ichi,Ishizu Takashi,Hirayama Kouichi,Gotoh Michihiro,Iitsuka Tadashi,Takemura Katsumi,Kikuchi Hiroshi,Nakamura Hideko,Kobayashi Masaki,Koyama Akio

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/15/3/385/23770500/150385.pdf

Reference21 articles.

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2. An overview of regular dialysis treatment in Japan (as of Dec. 31, 1998). Jpn Soc Dial Ther 1999; 64

3. Alcolado JC, Majid A, Brockington M, Sweeney MG, Morgan R, Rees A, Harding AE, Barnett AH. Mitochondrial gene defects in patients with NIDDM. Diabetologia1994; 37: 372–376

4. Kadowaki T, Kadowaki H, Mori Y et al. A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA. N Engl J Med1994; 330: 962–968

5. Kishimoto M, Hashiramoto M, Kanda F, Tanaka M, Kasuga M. Mitochondrial mutation in diabetic patient with gastrointestinal symptoms. Lancet1995; 345: 452 (Letter)

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