共 6 条
- [1] The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes:: evidence for heterogeneity of beta cell function among carriers of the R201H mutation DIABETOLOGIA, 2005, 48 (05) : 1029 - 1031
- [2] Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation Diabetologia, 2005, 48 : 2439 - 2441