Mutations of the TSH receptor as cause of congenital hyperthyroidism*-Reference-Cited by-同舟云学术

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Mutations of the TSH receptor as cause of congenital hyperthyroidism*

Published:2009-07-15 Issue:S 04 Volume:104 Page:124-128
ISSN:0947-7349
Container-title:Experimental and Clinical Endocrinology & Diabetes
language:en
Short-container-title:Exp Clin Endocrinol Diabetes

Author:

Schwab K. O.,Söhlemann P.,Gerlich M.,Broecker M.,Petrykowski W.,Holzapfel H. P.,Paschke R.,Grüters A.,Derwahl M.

Publisher

Georg Thieme Verlag KG

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0029-1211719

Cited by 33 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. Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene;Annals of Pediatric Endocrinology & Metabolism;2018-12-31

2. Receptor transduction pathways mediating hormone action;Pediatric Endocrinology;2014

3. Design of Super-arrestins for Gene Therapy of Diseases Associated with Excessive Signaling of G Protein-Coupled Receptors;Methods in Pharmacology and Toxicology;2013-12-24

4. Sporadic congenital nonautoimmune hyperthyroidism caused by P639S mutation in thyrotropin receptor gene;European Journal of Pediatrics;2012-02-28

5. Detection of combined genomic variants in a Jordanian family with familial non-autoimmune hyperthyroidism;Journal of Genetics;2009-07-28

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