A Novel Mechanism of Inherited TBG Deficiency: Mutation in a Liver-Specific Enhancer-Reference-Cited by-同舟云学术

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A Novel Mechanism of Inherited TBG Deficiency: Mutation in a Liver-Specific Enhancer

Published:2015-01 Issue:1 Volume:100 Page:E173-E181
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

Ferrara Alfonso Massimiliano,Pappa Theodora,Fu Jiao,Brown Christopher D.,Peterson April,Moeller Lars C.,Wyne Kathleen,White Kevin P.,Pluzhnikov Anna,Trubetskoy Vassily,Nobrega Marcelo,Weiss Roy E.,Dumitrescu Alexandra M.,Refetoff Samuel

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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