Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD)
✍ Scribed by PJ Guillausseau; D Dubois-Laforgue; P Massin; M Laloi-Michelin; C Bellanné-Chantelot; H Gin; E Bertin; JF Blickle; B Bauduceau; B Bouhanick; J Cahen-Varsaux; S Casanova; G Charpentier; P Chedin; C Derrien; A Grimaldi; B Guerci; E Kaloustian; F Lorenzini; A Murat; F Olivier; M Paques; V Paquis-Flucklinger; A Tielmans; M Vincenot; B Vialettes; J Timsit
- Book ID
- 117744504
- Publisher
- Masson Editeur
- Year
- 2004
- Tongue
- French
- Weight
- 85 KB
- Volume
- 30
- Category
- Article
- ISSN
- 1262-3636
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📜 SIMILAR VOLUMES
## Abstract ## Purpose To investigate high‐energy phosphate metabolism in striated skeletal muscle of patients with Maternally Inherited Diabetes and Deafness (MIDD) syndrome. ## Materials and Methods In 11 patients with the MIDD mutation (six with diabetes mellitus [DM] and five non‐DM) and eig