CORC  > 中国医学科学院 北京协和医学院
Genetic and functional analysis of two missense DUOX2 mutations in congenital hypothyroidism and goiter
Liu, Shiguo; Zhang, Wenhui; Zhang, Liqin; Zou, Hui; Lu, Kunna; Li, Qiang; Xia, Hongfei; Yan, Shengli; Ma, Xu
2018
卷号9期号:4页码:4366-4374
关键词congenital hypothyroidism DUOX2 DUOXA2 mutation function
ISSN号1949-2553
DOI10.18632/oncotarget.10525
URL标识查看原文
收录类别SCIE ; PUBMED
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/6346931
专题中国医学科学院 北京协和医学院
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GB/T 7714
Liu, Shiguo,Zhang, Wenhui,Zhang, Liqin,et al. Genetic and functional analysis of two missense DUOX2 mutations in congenital hypothyroidism and goiter[J],2018,9(4):4366-4374.
APA Liu, Shiguo.,Zhang, Wenhui.,Zhang, Liqin.,Zou, Hui.,Lu, Kunna.,...&Ma, Xu.(2018).Genetic and functional analysis of two missense DUOX2 mutations in congenital hypothyroidism and goiter.,9(4),4366-4374.
MLA Liu, Shiguo,et al."Genetic and functional analysis of two missense DUOX2 mutations in congenital hypothyroidism and goiter".9.4(2018):4366-4374.
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