CLINICAL CASE SEMINAR Extending the Clinical Heterogeneity of Iodide Transport Defect (ITD): A Novel Mutation R124H of the Sodium/Iodide Symporter Gene and Review of Genotype- Phenotype Correlations in ITD

Abstract

Pediatric Endocrine Unit, and Institut National de la Santé et de la Recherche Médicale, Equipe mixte INSERM 0363, Hôpital Necker Enfants-Malades (G.S., M.P.), 75743 Paris, France; Departments of Clinical Genetics and Medical Ethics, Kyoto University Graduate School of Medicine (S.K.), Kyoto 606-8501, Japan; Department of Endocrinology and Diabetes… (More)

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@inproceedings{Szinnai2006CLINICALCS, title={CLINICAL CASE SEMINAR Extending the Clinical Heterogeneity of Iodide Transport Defect (ITD): A Novel Mutation R124H of the Sodium/Iodide Symporter Gene and Review of Genotype- Phenotype Correlations in ITD}, author={Gabor Szinnai and Shinji Kosugi and Christ{\`e}le Derrien and Nadine Lucidarme and V{\'e}ronique David and Paul C Czernichow and Michel Polak}, year={2006} }