Author:
Sawada Hirotake,Inoue Shinobu,Sugimoto Tohru,Nagamachi Shigeki,Kosugi Shinji
Publisher
Japanese Society for Pediatric Endocrinology
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health
Reference14 articles.
1. 1) Wolff J. Congenital Goiter with defective iodide transport. Endocr Rev 1983; 4: 240-54.
2. 2) Stanbury JB, Dumont JE. Familial Goiter and related disorders. In: Stanbury JB, Wyngaarden JB, Fredrickson DS, Goldstein JL, Brown MS, eds. The Metabolic Basis of Inherited Disease. New York: McGraw-Hill, 1983; 231-69.
3. 3) Saito K, Yamamoto K, Yoshida S, Manabe S, et al. Goitrous hypothyroidism due to iodide-trapping defect. J Clin Endochnol Metab 1981; 53: 1267-72.
4. A Homozygous Missense Mutation of the Sodium/Iodide Symporter Gene Causing Iodide Transport Defect
5. High Prevalence of T354P Sodium/Iodide Symporter Gene Mutation in Japanese Patients with Iodide Transport Defect Who Have Heterogeneous Clinical Pictures