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Mosaic Paternal Uniparental Isodisomy and an ABCC8 Gene Mutation in a Patient With Permanent Neonatal Diabetes and Hemihypertrophy
Shield, J. P.H., Flanagan, S. E., Mackay, D. J., Harries, L. W., Proks, P., Girard, C., Ashcroft, F. M., Temple, I. K., Ellard, S.Volume:
57
Language:
english
Journal:
Diabetes
DOI:
10.2337/db07-0999
Date:
January, 2008
File:
PDF, 233 KB
english, 2008