6 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
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 |