Identification of a novel polymorphism in the fibronectin type II domain of the SEL1L gene and possible relation to the persistent hyperinsulinemic hypoglycemia of infancy
- 4 October 2004
- journal article
- Published by Elsevier in Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
- Vol. 554 (1-2) , 159-163
- https://doi.org/10.1016/j.mrfmmm.2004.04.007
Abstract
No abstract availableKeywords
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