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
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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