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 R2
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| Description | scientific article |
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author: Sian Ellard |
| Publication date | April 19, 2005 |
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