A novel heterozygous IGF-1 receptor mutation associated with hypoglycemia

Mutation in the insulin-like growth factor-1 receptor (IGF1R) gene is a rare cause for intrauterine and postnatal growth disorders. Patients identified with IGF1R mutations present with either normal or impaired glucose tolerance. None of the cases described so far showed hypoglycemia. We aimed to i...

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Detalles Bibliográficos
Autores principales: Solomon-Zemler, R, Basel-Vanagaite, L, Steier, D, Yakar, S, Mel, E, Phillip, M, Bazak, L, Bercovich, D, Werner, H, de Vries, L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5551424/
https://www.ncbi.nlm.nih.gov/pubmed/28649085
http://dx.doi.org/10.1530/EC-17-0038

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5551424/
https://www.ncbi.nlm.nih.gov/pubmed/28649085
http://dx.doi.org/10.1530/EC-17-0038

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