Genetic analysis of iodide transporter and recycling (NIS, PDS, SLC26A7, IYD) in patients with congenital hypothyroidism

Author:

Li Miaomiao,Li Xiaole,Wang Fang,Ren Yubao,Zhang Xiao,Wang Jingli,Shen Lu,Zhao Dehua,ShiguoLiu

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference39 articles.

1. Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7;Acar;J Endocrinol Invest.,2021

2. Molecular characterization of iodotyrosine dehalogenase deficiency in patients with hypothyroidism;Afink;J Clin Endocrinol Metab.,2008

3. The Placenta as a Compensatory Iodine Storage Organ;Burns;Thyroid.,2011

4. Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations;Campbell;Hum Mutat.,2001

5. Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism. JCI;Cangul;Insight.,2018

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