High Frequency of D727E Polymorphisms in Exon 10 of the TSHR Gene in Brazilian Patients with Congenital Hypothyroidism-Reference-Cited by-同舟云学术

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High Frequency of D727E Polymorphisms in Exon 10 of the TSHR Gene in Brazilian Patients with Congenital Hypothyroidism

Published:2010-01 Issue:12 Volume:23 Page:
ISSN:0334-018X
Container-title:Journal of Pediatric Endocrinology and Metabolism
language:
Short-container-title:

Author:

Alves Erik A. C.,Cruz Cleber M.,Pimentel Clebson P.,Ribeiro Rita C. M.,Santos Andrea K. C. R.,Caldato Milena C. F.,Santana-da-Silva Luiz C.

Publisher

Walter de Gruyter GmbH

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Link

https://www.degruyter.com/document/doi/10.1515/jpem.2010.206/pdf

Reference31 articles.

1. The W546X Mutation of the Thyrotropin Receptor Gene: Potential Major Contributor to Thyroid Dysfunction in a Caucasian Population

Cited by 8 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. Congenital Hypothyroidism Patients With Thyroid Hormone Receptor Variants Are Not Rare: A Systematic Review;INQUIRY: The Journal of Health Care Organization, Provision, and Financing;2021-01

2. Receptor Transduction Pathways Mediating Hormone Action;Sperling Pediatric Endocrinology;2021

3. The rs1991517 polymorphism is a genetic risk factor for congenital hypothyroidism;3 Biotech;2020-06

4. Mutation screening in the genes PAX-8, NKX2-5, TSH-R, HES-1 in cohort of 63 Brazilian children with thyroid dysgenesis;Archives of Endocrinology and Metabolism;2018-08

5. Evaluation of the tshr gene reveals polymorphisms associated with typical symptoms in primary congenital hypothyroidism;Journal of Pediatric Endocrinology and Metabolism;2016-01-01

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