Correlation of DUOX2 residual enzymatic activity with phenotype in congenital hypothyroidism caused by biallelic DUOX2 defects

Correlation of DUOX2 residual enzymatic activity with phenotype in congenital hypothyroidism caused by biallelic DUOX2 defects
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双等位基因所致先天性甲状腺功能减退症DUOX2残留酶活性与表型的相关性

DOI:
10.1111/cge.14065
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发表时间:
2021-09
期刊:
影响因子:
3.5
通讯作者:
Song HD
Song HD
中科院分区:
医学2区
文献类型:
--
作者:
Sun F;Zhang RJ;Cheng F;Fang Y;Yang RM;Ye XP;Han B;Zhao SX;Dong M;Song HD

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DUOX2是中国先天性甲状腺功能减退症(CH)患者中最常见的突变基因。然而,在DUOX2突变患者中没有发现可靠的基因型-表型关系。本研究在266c中筛选了DUOX2突变
DUOX2 is the most frequently mutated gene in patients with congenital hypothyroidism (CH) in China. However, no reliable genotype–phenotype relationship has been found in patients with DUOX2 mutations. In this study, DUOX2 mutations were screened in 266 C
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