A Missense Mutation G2320R in the Thyroglobulin Gene Causes Non-goitrous Congenital Primary Hypothyroidism in the WIC-rdwRat-Reference-Cited by-同舟云学术

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A Missense Mutation G2320R in the Thyroglobulin Gene Causes Non-goitrous Congenital Primary Hypothyroidism in the WIC-rdwRat

Published:2000-12 Issue:12 Volume:14 Page:1944-1953
ISSN:0888-8809
Container-title:Molecular Endocrinology
language:en
Short-container-title:Molecular Endocrinology

Author:

Kim Paul S.,Ding Ming,Menon Shekar,Jung Cha-Gyun,Cheng Ji-Ming,Miyamoto Tomomi,Li Bailing,Furudate Sen-ichi,Agui Takashi

Publisher

The Endocrine Society

Subject

Endocrinology,Molecular Biology,General Medicine

Cited by 40 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

1. Positional cloning of rat mutant genes reveals new functions of these genes;Experimental Animals;2023

2. The p.Pro2232Leu variant in the ChEL domain of thyroglobulin gene causes intracellular transport disorder and congenital hypothyroidism;Endocrine;2022-12-22

3. Defective Thyroglobulin: Cell Biology of Disease;International Journal of Molecular Sciences;2022-11-06

4. The p.Pro2232Leu variant in the ChEL domain of thyroglobulin gene causes intracellular transport disorder and congenital hypothyroidism.;2022-10-31

5. Comparative analysis of human and bovine thyroglobulin structures;Journal of Analytical Science and Technology;2022-07-25

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