reference/10659570

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10659570

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endingPage	E502
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publicationName	The Journal of clinical endocrinology and metabolism
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bibliographicCitation	Flanagan SE, Patch AM, Locke JM, Akcay T, Simsek E, Alaei M, Yekta Z, Desai M, Kapoor RR, Hussain K, Ellard S. Genome-wide homozygosity analysis reveals HADH mutations as a common cause of diazoxide-responsive hyperinsulinemic-hypoglycemia in consanguineous pedigrees. J Clin Endocrinol Metab. 2011 Mar;96(3):E498–502. PMID: 21252247; PMCID: PMC3100671.
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date	2011-03-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/21252247 https://pubmed.ncbi.nlm.nih.gov/PMC3100671 https://doi.org/10.1210/jc.2010-1906
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Genome-Wide Homozygosity Analysis Reveals HADH Mutations as a Common Cause of Diazoxide-Responsive Hyperinsulinemic-Hypoglycemia in Consanguineous Pedigrees
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