P Massin, M Virally-Monod, B Vialettes, M … - Ophthalmology, 1999 - Elsevier Forty-six patients from 29 families with an adenine-to-guanine mutation of
mitochondrial DNA were recruited from a French collaborative multicenter study.
Thirty-five patients had MIDD, 8 were asymptomatic children of MIDD ... Cited by 34 - Related articles - BL Direct - All 6 versions
PJ Saker, AT Hattersley, B Barrow, MS … - Diabetic Medicine, 1997 - interscience.wiley.com Some patients with Type 2 (non-insulin-dependent) diabetes mellitus possess a
mitochondrial mutation in the tRNA Leu(UUR) gene at position 3243 bp. These
subjects show a maternal mode of inheritance and often have hearing ... Cited by 34 - Related articles - BL Direct - All 14 versions
- ►asnjournals.org B Guery, G Choukroun, LH Noel, P Clavel, A … - Journal of the American Society of Nephrology, 2003 - Am Soc Nephrol *Service de Néphrologie and INSERM U507, Hôpital Necker, Paris; Service de
Néphrologie, Hôpital Sud, Amiens; Service de Néphrologie, Hôpital de
Brabois, Vandoeuvre-lès-Nancy; Département de Génétique Médicale and ... Cited by 31 - Related articles - BL Direct - All 7 versions
JMW Van den Ouweland, H Lemkes, W … - Nature Genetics, 1992 - nature.com Non−insulin−dependent (type II) diabetes mellitus (NIDDM) is characterized
by hyperglycaemia and insulin resistance, and affects nearly 5% of the general
population. Inherited factors are important for its development, but the ... Cited by 612 - Related articles - All 3 versions
LM Hart, JJ Jansen, HHPJ Lemkes, P Knijff, … - Human Mutation, 1996 - interscience.wiley.com We showed previously that a mutation in the mitochondrial tRNA Leu(UUR) gene at
position 3243 associates with maternally inherited diabetes and deafness (MIDD).
This mutation shows heteroplasmy in DNA from peripheral blood and other ... Cited by 46 - Related articles - BL Direct - All 2 versions
H Katagiri, I Asano, H Ishihara, K Inukai, M … - Diabetologia, 1994 - Springer Summary Mutations in the mitochondrial gene were recently identified in a large
pedigree of diabetes mel- litus and deafness. As the mitochondrial gene is
mater- nally inherited, Japanese diabetic patients whose mo- thers were ... Cited by 79 - Related articles - BL Direct - All 3 versions
S Suzuki, Y Hinokio, M Ohtomo, M Hirai, A … - Diabetologia, 1998 - Springer 4]. The clinical features of diabetes mellitus with the 3243 bp mutation are
maternal inheritance, progres- sive insulin secretory defect and a high
association with neurosensory deafness. The 3243 bp mutation was identified ... Cited by 51 - Related articles - BL Direct - All 4 versions
PR Smith, SC Bain, PA Good, AT Hattersley, … - Ophthalmology, 1999 - Elsevier To study the association of retinal disease and the syndrome of maternally
inherited diabetes and deafness caused by an A to G mutation in the tRNA leucine
gene at base pair 3243 (A3243G) of the mitochondrial genome. Cited by 24 - Related articles - BL Direct - All 11 versions
