Neonatal Diabetes and Congenital Malabsorptive Diarrhea Attributable to a Novel Mutation in the Human Neurogenin-3 Gene Coding Sequence

OBJECTIVE: The aim was to describe the clinical presentation and to characterize the genetic mutation present in a child with congenital malabsorptive diarrhea and neonatal diabetes. RESEARCH DESIGN AND METHODS: Clinical data were obtained from chart review. Histopathological characterization of int...

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Bibliographic Details
Main Authors: Pinney, Sara E., Oliver-Krasinski, Jennifer, Ernst, Linda, Hughes, Nkecha, Patel, Puja, Stoffers, Doris A., Russo, Pierre, De León, Diva D.
Format: Artigo
Language:Inglês
Published: Endocrine Society 2011
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Special Features
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3135203/
https://ncbi.nlm.nih.gov/pubmed/21490072
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2011-0029
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