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Delayed onset congenital hypothyroidism in a patient with DUOX2 mutations and maternal iodine excess
Kasahara, Toshihiko, Narumi, Satoshi, Okasora, Keisuke, Takaya, Ryuzo, Tamai, Hiroshi, Hasegawa, TomonobuVolume:
161
Language:
english
Journal:
American Journal of Medical Genetics Part A
DOI:
10.1002/ajmg.a.35693
Date:
January, 2013
File:
PDF, 146 KB
english, 2013