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The identification of a R201H mutation inKCNJ11, 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

✍ Scribed by T. Klupa; E. L. Edghill; J. Nazim; J. Sieradzki; S. Ellard; A. T. Hattersley; M. T. Malecki


Publisher
Springer
Year
2005
Tongue
English
Weight
78 KB
Volume
48
Category
Article
ISSN
0012-186X

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