Hyperinsulinism of Infancy: Novel ABCC8 and KCNJ11 Mutations and Evidence for Additional Locus Heterogeneity

S Tornovsky, A Crane, KE Cosgrove… - The Journal of …, 2004 - academic.oup.com
Hyperinsulinism of infancy is a genetically heterogeneous disease characterized by
dysregulation of insulin secretion resulting in severe hypoglycemia. To date, mutations in …
被引用次数：97 相关文章

Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity.

S Tornovsky, A Crane, KE Cosgrove… - The Journal of …, 2004 - europepmc.org
Hyperinsulinism of infancy is a genetically heterogeneous disease characterized by
dysregulation of insulin secretion resulting in severe hypoglycemia. To date, mutations in …

Hyperinsulinism of infancy: Novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity

S Tornovsky, A Crane… - Journal of Clinical …, 2004 - research.manchester.ac.uk
Hyperinsulinism of infancy is a genetically heterogeneous disease characterized by
dysregulation of insulin secretion resulting in severe hypoglycemia. To date, mutations in …

[引用][C] Hyperinsulinism of infancy: Novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity

S TORNOVSKY, A CRANE, E NAHARI… - The Journal of …, 2004 - pascal-francis.inist.fr
Hyperinsulinism of infancy: Novel ABCC8 and KCNJ11 mutations and evidence for
additional locus heterogeneity CNRS Inist Pascal-Francis CNRS Pascal and Francis …
[PDF] archive.org

[PDF][PDF] Hyperinsulinism of Infancy: Novel ABCC8 and KCNJ11 Mutations and Evidence for Additional Locus Heterogeneity

The Journal of Clinical Endocrinology & Metabolism - scholar.archive.org
SHARONA TORNOVSKY, ANA CRANE, KAREN E. COSGROVE, KHALID HUSSAIN,
JUDITH LAVIE, MA'AYAN HEYMAN, YARON NESHER, NA'AMA KUCHINSKI, ETTI BEN …

Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity

S Tornovsky, A Crane, KE Cosgrove… - The Journal of …, 2004 - pubmed.ncbi.nlm.nih.gov
Hyperinsulinism of infancy is a genetically heterogeneous disease characterized by
dysregulation of insulin secretion resulting in severe hypoglycemia. To date, mutations in …
[PDF] academia.edu

[PDF][PDF] Hyperinsulinism of Infancy: Novel ABCC8 and KCNJ11 Mutations and Evidence for Additional Locus Heterogeneity

The Journal of Clinical Endocrinology & Metabolism - academia.edu
SHARONA TORNOVSKY, ANA CRANE, KAREN E. COSGROVE, KHALID HUSSAIN,
JUDITH LAVIE, MA'AYAN HEYMAN, YARON NESHER, NA'AMA KUCHINSKI, ETTI BEN …
[PDF] academia.edu

[PDF][PDF] Hyperinsulinism of Infancy: Novel ABCC8 and KCNJ11 Mutations and Evidence for Additional Locus Heterogeneity

The Journal of Clinical Endocrinology & Metabolism - academia.edu
SHARONA TORNOVSKY, ANA CRANE, KAREN E. COSGROVE, KHALID HUSSAIN,
JUDITH LAVIE, MA'AYAN HEYMAN, YARON NESHER, NA'AMA KUCHINSKI, ETTI BEN …

[引用][C] Hyperinsulinism of infancy: Novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity

S TORNOVSKY, A CRANE… - The Journal of …, 2004 - Endocrine Society