Concepedia

Publication | Open Access

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

16

Citations

17

References

2000

Year

Abstract

We found that a mitochondrial gene mutation at nucleotide 3243 was present in one dialysis patient with NIDDM and deafness. The prevalence of this mutation was found to be below 1% in diabetic end-stage renal disease patients in Japan.

References

YearCitations

1981

9.6K

1990

2.1K

1994

559

1997

118

1994

81

1994

77

1996

66

1993

58

2009

54

1995

49

Page 1