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A novel multi–system syndrome of neonatal diabetes, developmental delay and epilepsy is defined by mutations in the PNDM2 gene

Document Type

Academic Journal

Author

Hattersley, A. T.; Pearson, E. R.; Sumnik, Z.; Bruining, G. J.; Slingerland, A. S.; van Rhijn, A.; Wales, J. K. H.; Temple, I. K.; Mackay, D.; Shield, J. P. H.; Edghill, E. L.; Clark, P.; Ellard, S.; Njølstad, P. R.; Gloyn, A. L.

Source

Diabetic Medicine Supplement. Apr 01, 2004 21 Suppl 2:8-9

Subject

Language

English

ISSN

1466-5468

Online Access

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