t/gene-duox2

DUOX2 gene

Discuss publications and research concerning the DUOX2 gene.

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Related literature

Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic-ischemic encephalopathy: A retrospective analysis.
DUOX2
Conformation of the N-Terminal Ectodomain Elicits Different Effects on DUOX Function: A Potential Impact on Congenital Hypothyroidism Caused by a H2O2 Production Defect.
DUOX2
[Transient congenital hypothyroidism due to biallelic defects of DUOX2 gene. Two clinical cases].
DUOX2
Next-generation sequencing analysis of twelve known causative genes in congenital hypothyroidism.
DUOX2
[Characteristics of DUOXA2 gene mutation in children with congenital hypothyroidism].
DUOX2
Mutation screening of DUOX2 in Chinese patients with congenital hypothyroidism.
DUOX2
Heterogeneous phenotype in children affected by non-autoimmune hypothyroidism: an update.
DUOX2
Defects of thyroidal hydrogen peroxide generation in congenital hypothyroidism.
DUOX2
[The thyroid as a model for molecular mechanisms in genetic diseases].
DUOX2

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