Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[DUOX2 mutations in children with congenital hypothyroidism].

Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics - 1 Jan 2015

Chai Jian, Yang Xiao-Long, Guo Ming-Zhen, Liu Lu, Liu Shi-Guo, Yan Sheng-Li, Ge Yin-Lin

Abstract excerpt

OBJECTIVE: To study the features of DUOX2 mutations and genotype-phenotype relationship in children with congenital hypothyroidism (CH), in order to provide evidence for gene diagnosis and gene treatment of CH. METHODS: Blood samples were collected from 10 CH children with thyromegaly. Genomic DNA was extracted from peripheral blood leukocytes. All exons of DUOX2 gene were analyzed using PCR and direct...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child
Share to Child, Preschool
Share to Computational Biology

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Congenital Hypothyroidism

Share to Dual Oxidases

Share to Mutation

Share to NADPH Oxidases

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 25616291

Genes

DUOX2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[DUOX2 mutations in children with congenital hypothyroidism].PMID 25616291Read ↗

[DUOX2 gene mutation in patients with congenital goiter with hypothyroidism].Semantic proximity Read ↗

Mutation Screening of DUOX2 Gene in Children with Congenital HypothyroidismSemantic proximity Read ↗

[Characteristics of DUOXA2 gene mutation in children with congenital hypothyroidism].Semantic proximity Read ↗

The Prevalence, Clinical, and Molecular Characteristics of Congenital Hypothyroidism Caused by DUOX2 Mutations: A Population-Based Cohort Study in Guangzhou.Semantic proximity Read ↗

A Novel c.554+5C>T Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism.Semantic proximity Read ↗

Identification and analyzes of DUOX2 mutations in two familial congenital hypothyroidism cases.Semantic proximity Read ↗

Clinical and molecular characteristics of congenital hypothyroidism with DUOX2 mutationsSemantic proximity Read ↗

Mutation screening of DUOX2 in Chinese patients with congenital hypothyroidism.Semantic proximity Read ↗

High prevalence of DUOX2 gene mutations among children with congenital hypothyroidism in central China.Semantic proximity Read ↗

Genotypes and phenotypes of congenital goitre and hypothyroidism caused by mutations in dual oxidase 2 genes.Semantic proximity Read ↗

DUOX2 Mutations Are Frequently Associated With Congenital Hypothyroidism in the Korean Population.Semantic proximity Read ↗

High prevalence of DUOX2 mutations in Japanese patients with permanent congenital hypothyroidism or transient hypothyroidism.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.