Iodides

dual oxidase 2 ; Homo sapiens







6 Article(s)
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1 26506010 Compound heterozygous DUOX2 gene mutations (c.2335-1G>C/c.3264_3267delCAGC) associated with congenital hypothyroidism. Characterization of complex cryptic splice sites by minigene analysis. 2016 Jan 5 2
2 22301785 Mice deficient in dual oxidase maturation factors are severely hypothyroid. 2012 Mar 1
3 21367925 A single copy of the recently identified dual oxidase maturation factor (DUOXA) 1 gene produces only mild transient hypothyroidism in a patient with a novel biallelic DUOXA2 mutation and monoallelic DUOXA1 deletion. 2011 May 1
4 16322276 Three mutations (p.Q36H, p.G418fsX482, and g.IVS19-2A>C) in the dual oxidase 2 gene responsible for congenital goiter and iodide organification defect. 2006 Feb 2
5 16987011 Physiology and pathophysiology of the DUOXes. 2006 Sep-Oct 2
6 12110737 Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidism. 2002 Jul 11 2