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Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case–control study

✍ Scribed by P. Massin; D. Dubois-Laforgue; T. Meas; M. Laloi-Michelin; H. Gin; B. Bauduceau; C. Bellanné-Chantelot; E. Bertin; J.-F. Blickle; B. Bouhanick; J. Cahen-Varsaux; S. Casanova; G. Charpentier; P. Chedin; O. Dupuy; A. Grimaldi; B. Guerci; E. Kaloustian; A. Lecleire-Collet; F. Lorenzini; A. Murat; H. Narbonne; F. Olivier; V. Paquis-Flucklinger; M. Virally; M. Vincenot; B. Vialettes; J. Timsit; P. J. Guillausseau; for the GEDIAM (Mitochondrial Diabetes French Study Group)

Publisher: Springer
Year: 2008
Tongue: English
Weight: 139 KB
Volume: 51
Category: Article
ISSN: 0012-186X
DOI: 10.1007/s00125-008-1073-1

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