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5 in total

1. A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

Authors: Y Goto; I Nonaka; S Horai
Journal: Nature Date: 1990-12-13 Impact factor: 49.962

2. Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples.

Authors: S R Hammans; M G Sweeney; M Brockington; J A Morgan-Hughes; A E Harding
Journal: Lancet Date: 1991-06-01 Impact factor: 79.321

3. Prevalence of mitochondrial gene mutations in families with diabetes mellitus.

Authors: N Vionnet; P Passa; P Froguel
Journal: Lancet Date: 1993-12-04 Impact factor: 79.321

4. Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness.

Authors: J M van den Ouweland; H H Lemkes; W Ruitenbeek; L A Sandkuijl; M F de Vijlder; P A Struyvenberg; J J van de Kamp; J A Maassen
Journal: Nat Genet Date: 1992-08 Impact factor: 38.330

5. Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA.

Authors: W Reardon; R J Ross; M G Sweeney; L M Luxon; M E Pembrey; A E Harding; R C Trembath
Journal: Lancet Date: 1992-12-05 Impact factor: 79.321

5 in total

2 in total

1. Selection of primers for detection of A to G mutation at nucleotide 3243 of the mitochondrial gene.

Authors: M Odawara; K Sasaki; Y Tachi; K Yamashita
Journal: Diabetologia Date: 1995-03 Impact factor: 10.122

2. Detection of mitochondrial DNA mutations in patients with diabetes mellitus.

Authors: A W Thomas; R Morgan; A Majid; A Rees; J C Alcolado
Journal: Diabetologia Date: 1995-03 Impact factor: 10.122

2 in total