Brief Report: A Novel Sodium/Iodide Symporter Mutation, S356F, Causing Congenital Hypothyroidism.

Author:

Durgia Harsh1,Nicholas Adeline K.2,Schoenmakers Erik3,Dickens Jennifer A4,Halanaik Dhanapathi5,Sahoo Jayaprakash1,Kamalanathan Sadishkumar1,Schoenmakers Nadia6

Affiliation:

1. Jawaharlal Institute of Postgraduate Medical Education and Research, 29988, Department of Endocrinology, Puducherry, Tamil Nadu, India, ;

2. University of Cambridge, University of Cambridge Metabolic Research Laboratories, Level 4, Wellcome Trust-MRC Institute of Metabolic Science, Box 289, Addenbrooke’s Hospital, Cambridge, Cambridge, United Kingdom of Great Britain and Northern Ireland, CB2 0QQ, ;

3. Institute of Metabolic Science, Addenbrooke's Hospital, Metabolic Research Laboratories, University of Cambridge Metabolic Research Laboratories, Level 4, Wellcome Trust-MRC Institute of Metabolic Science, Box 289, Addenbrooke’s Hospital, Cambridge, United Kingdom of Great Britain and Northern Ireland, CB2 0QQ, ;

4. Cambridge Institute for Medical Research, 98524, Cambridge, Cambridgeshire, United Kingdom of Great Britain and Northern Ireland, ;

5. Jawaharlal Institute of Postgraduate Medical Education and Research, 29988, Department of Nuclear Medicine, Puducherry, Tamil Nadu, India, ;

6. University of Cambridge, 2152, Institute of Metabolic Science, Box 289, Addenbrooke's Hospital, Hills Road, Cambridge, Cambridge, United Kingdom of Great Britain and Northern Ireland, CB2 1TN, ;

Publisher

Mary Ann Liebert Inc

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

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