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 (Q46444395)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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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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 (English)
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T Klupa
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E L Edghill
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J Nazim
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J Sieradzki
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A T Hattersley
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M T Malecki
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19 April 2005
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48
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5
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1029-1031
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