Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation. - Velho,G.; Byrne,M.M.; Clement,K.; Sturis,J.; Pueyo,M.E.; Blanche,H.; Vionnet,N.; Fiet,J.; Passa,P.; Robert,J.J.; Polonsky,K.S.; Froguel,P. (Diabetes, 1996)