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Heterogeneity in disease severity in a family with a novel G68V GCK activating mutation causing persistent hyperinsulinaemic hypoglycaemia of infancy

✍ Scribed by M. Wabitsch; G. Lahr; M. Van de Bunt; C. Marchant; M. Lindner; J. Von Puttkamer; A. Fenneberg; K. M. Debatin; R. Klein; S. Ellard; A. Clark; A. L. Gloyn


Book ID
110925265
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
756 KB
Volume
24
Category
Article
ISSN
0742-3071

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