High prevalence of DUOX2 mutations in Japanese patients...

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Journal of Pediatric Endocrinology and Metabolism 2016 / 01

High prevalence of DUOX2 mutations in Japanese patients with permanent congenital hypothyroidism or transient hypothyroidism

Matsuo, Kumihiro, Tanahashi, Yusuke, Mukai, Tokuo, Suzuki, Shigeru, Tajima, Toshihiro, Azuma, Hiroshi, Fujieda, Kenji
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Language:
english
Journal:
Journal of Pediatric Endocrinology and Metabolism
DOI:
10.1515/jpem-2015-0400
Date:
January, 2016
File:
PDF, 165 KB
english, 2016
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