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Molecular basis of Kir6.2 mutations causing neonatal diabetes and neonatal diabetes with neurological features

Publication status:: Published

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APA Style

Proks, P., Antcliff, J., Gloyn, A., Hattersley, A., & Ashcroft, F. (2005). Molecular basis of Kir6.2 mutations causing neonatal diabetes and neonatal diabetes with neurological features. 88(1), 181A–181A.

MLA Style

Proks, P, et al. “Molecular Basis of Kir6.2 Mutations Causing Neonatal Diabetes and Neonatal Diabetes with Neurological Features.” vol. 88, no. 1, 2005, pp. 181A–181A.

Chicago Style

Proks, P, J Antcliff, A Gloyn, A Hattersley, and F Ashcroft. 2005. “Molecular Basis of Kir6.2 Mutations Causing Neonatal Diabetes and Neonatal Diabetes with Neurological Features.” 88 (1): 181A–181A.
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Authors

+ Proks, P More by this author

Role:: Author

+ Antcliff, J More by this author

Role:: Author

+ Gloyn, A More by this author

Role:: Author

+ Hattersley, A More by this author

Role:: Author

+ Ashcroft, F More by this author

Institution:: University of Oxford
Division:: MSD
Department:: Physiology Anatomy & Genetics
Role:: Author

Host title:: BIOPHYSICAL JOURNAL
Volume:: 88
Issue:: 1
Pages:: 181A-181A
Publication date:: 2005-01-01
ISSN:: 0006-3495

Pubs id:: pubs:114615
UUID:: uuid:f1eecfc5-ffaf-492d-8fd2-8c9e40facee0
Local pid:: pubs:114615
Source identifiers:: 114615
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_f1eecfc5ffaf492d8fd28c9e40facee0

Terms of use

Copyright date:: 2005

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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