How to Cite this Article: Kasahara T, Narumi S, Okasora K, Takaya R, Tamai H, Hasegawa T. 2012. Delayed onset congenital hypothyroidism in a patient with DUOX2 mutations and maternal iodine excess. Am J Med Genet Part A 161A:214–217.
Version of Record online: 14 DEC 2012
Copyright © 2012 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 1, pages 214–217, January 2013
How to Cite
Kasahara, T., Narumi, S., Okasora, K., Takaya, R., Tamai, H. and Hasegawa, T. (2013), Delayed onset congenital hypothyroidism in a patient with DUOX2 mutations and maternal iodine excess. Am. J. Med. Genet., 161: 214–217. doi: 10.1002/ajmg.a.35693
Toshihiko Kasahara and Satoshi Narumi contributed equally to this work.
Conflict of interest: None.
- Issue online: 22 DEC 2012
- Version of Record online: 14 DEC 2012
- Manuscript Accepted: 17 JUN 2012
- Manuscript Received: 12 APR 2012
- The Japan Society for the Promotion of Science
- The Ministry of Health, Labour and Welfare, Japan
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