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Permanent Neonatal Diabetes Mellitus Caused by a Novel Homozygous (T168A) Glucokinase (GCK) Mutation: Initial Response to Oral Sulphonylurea Therapy

✍ Scribed by Doga Turkkahraman; Iffet Bircan; Nicholas D. Tribble; Sema Akçurin; Sian Ellard; Anna L. Gloyn


Book ID
113744502
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
350 KB
Volume
153
Category
Article
ISSN
1097-6833

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