Varaico: Literature-Extracted Genetic Variants

Gene:DUOX2
Variant:p.K1360_L1361Splc
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DUOX2

NM_001363711.2:p.K1360_L1361Splc

Associated Papers

Analysis of Worldwide Carrier Frequency and Predicted Genetic Prevalence of Autosomal Recessive Congenital Hypothyroidism Based on a General Population Database.

Park KS

Genes, 2021

34200080 (PubMed )
Supplement: genes-12-00863-s001.zip › Supplementary_Files_Rev1_v20210529_.xlsx › Table_S6

A clinically euthyroid child with a large goiter due to a thyroglobulin gene defect: clinical features and genetic studies.

Hermanns P et al.

Journal of Pediatric Endocrinology & Metabolism : Jpem, 2013

Thyroglobulin gene mutations in congenital hypothyroidism.

Targovnik HM et al.

Hormone Research in Paediatrics, 2011

Genetics and phenomics of hypothyroidism and goiter due to thyroglobulin mutations.

Targovnik HM et al.

Molecular and Cellular Endocrinology, 2010

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."