Open AccessGenotype and phenotype correlation in a cohort of Chinese congenital hypothyroidism patients with DUOX2 mutations
Author(s) -
Zhangqian Zheng,
Lin Yang,
Chengjun Sun,
Jing Wu,
Feihong Luo,
Wenhao Zhou,
Wei Lu
Publication year - 2020
Publication title -
annals of translational medicine
Language(s) - English
Resource type - Journals
eISSN - 2305-5847
pISSN - 2305-5839
DOI - 10.21037/atm-20-7165
Subject(s) - medicine , newborn screening , cohort , genotype , congenital hypothyroidism , pediatrics , exome sequencing , subclinical infection , phenotype , mutation , thyroid , compound heterozygosity , genotype phenotype distinction , endocrinology , genetics , gastroenterology , biology , gene
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