Donohue Syndrome in a Neonate with Homozygous Deletion of Exon 3 of the Insulin Receptor Gene
Author:
Publisher
Walter de Gruyter GmbH
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health
Link
https://www.degruyter.com/document/doi/10.1515/JPEM.2009.22.7.669/pdf
Reference29 articles.
1. Syndromes d'insulinorésistance extrême génétiquement déterminés
2. Plasma Adiponectin as a Marker of Insulin Receptor Dysfunction
3. Clinical Course of the Syndrome of Autoantibodies to the Insulin Receptor (Type B Insulin Resistance)
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