Mutations in the liver glycogen synthase gene in children with hypoglycemia due to glycogen storage disease type 0.

Por Orho, M, Bosshard, N U, Buist, N R, Gitzelmann, R, Aynsley-Green, A, Blümel, P, Gannon, M C, Nuttall, F Q, Groop, L C
Publicado em 1998

Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect.

Por Lehto, M, Tuomi, T, Mahtani, M M, Widén, E, Forsblom, C, Sarelin, L, Gullström, M, Isomaa, B, Lehtovirta, M, Hyrkkö, A, Kanninen, T, Orho, M, Manley, S, Turner, R C, Brettin, T, Kirby, A, Thomas, J, Duyk, G, Lander, E, Taskinen, M R, Groop, L
Publicado em 1997