Recessive mutations in the INS gene; a novel common cause of permanent neonatal diabetes in consanguineous pedigrees

Edghill, E. L., Locke, J., Flanagan, S. E., Patch, A. M., Harries, L. W., Ellard, S. and Hattersley, A. T. (2008). Recessive mutations in the INS gene; a novel common cause of permanent neonatal diabetes in consanguineous pedigrees. In: Abstracts of the 44th EASD Annual Meeting of the European Association for the Study of Diabetes. 44th EASD Annual Meeting of the European Association for the Study of Diabetes, Rome, Italy, (S104-S104). 8-11 September 2008. doi:10.1007/s00125-008-1117-6


Author Edghill, E. L.
Locke, J.
Flanagan, S. E.
Patch, A. M.
Harries, L. W.
Ellard, S.
Hattersley, A. T.
Title of paper Recessive mutations in the INS gene; a novel common cause of permanent neonatal diabetes in consanguineous pedigrees
Conference name 44th EASD Annual Meeting of the European Association for the Study of Diabetes
Conference location Rome, Italy
Conference dates 8-11 September 2008
Proceedings title Abstracts of the 44th EASD Annual Meeting of the European Association for the Study of Diabetes   Check publisher's open access policy
Journal name Diabetologia   Check publisher's open access policy
Place of Publication Heidelberg, Germany
Publisher Springer
Publication Year 2008
Sub-type Published abstract
DOI 10.1007/s00125-008-1117-6
ISSN 0012-186X
1432-0428
Volume 51
Issue Suppl. 1
Start page S104
End page S104
Total pages 1
Language eng
Q-Index Code EX
Q-Index Status Provisional Code
Institutional Status Unknown

Document type: Conference Paper
Collection: Institute for Molecular Bioscience - Publications
 
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