HuGE Literature Finder
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Records 1-6
High prevalence of DUOX2 mutations in Japanese patients with permanent congenital hypothyroidism or transient hypothyroidism.
Journal of pediatric endocrinology & metabolism : JPEM 2016 May . Matsuo Kumihiro, Tanahashi Yusuke, Mukai Tokuo, Suzuki Shigeru, Tajima Toshihiro, Azuma Hiroshi, Fujieda Ken |
DUOX2 Mutations Are Frequently Associated With Congenital Hypothyroidism in the Korean Population.
Annals of laboratory medicine 2016 Mar 36 (2): 145-53. Park Kyoung Jin, Park Hyun Kyung, Kim Young Jin, Lee Kyoung Ryul, Park Jong Ho, Park June Hee, Park Hyung Doo, Lee Soo Youn, Kim Jong W |
Heterozygous Mutations of the DUOXA2 and DUOX2 Genes in Dizygotic Twins with Congenital Hypothyroidism.
Clinical laboratory 2016 62 (5): 849-54. Yang Liu-Xue, Ma Shao-Gang, Qiu Ya-Li, Zheng Xi |
Novel c.554+5C>T Mutation in the DUOXA2 gene Combinated with p.R885Q Mutation in the DUOX2 Gene Causes Congenital Hypothyroidism.
Journal of clinical research in pediatric endocrinology 2015 Dec . Zheng Xiao, Ma Shao Gang, Qiu Ya Li, Guo Man Li, Shao Xiao Ju |
Novel genetic variants in the TPO gene cause congenital hypothyroidism.
Scandinavian journal of clinical and laboratory investigation 2015 Jul 1-5. Ma Shao-Gang, Qiu Ya-Li, Zhu Hong, Liu Hong, Li Qing, Ji Chun-M |
A novel dual oxidase maturation factor 2 gene mutation for congenital hypothyroidism.
International journal of molecular medicine 2012 Dec . Yi RH, Zhu WB, Yang LY, Lan L, Chen Y, Zhou JF, Wang J, Su YQ |
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- Page last updated:Dec 5, 2019
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