Genotype and phenotype correlation in a cohort of Chinese congenital hypothyroidism patients with DUOX2 mutations

BACKGROUND: This study aimed to explore the relationship between the phenotype and genotype of congenital hypothyroidism (CH) caused by dual oxidase 2 (DUOX2) mutation in Chinese children, and to investigate the genetic causes of permanent and transient hypothyroidism through next-generation genetic...

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Detalles Bibliográficos
Autores principales: Zheng, Zhangqian, Yang, Lin, Sun, Chengjun, Wu, Jing, Luo, Feihong, Zhou, Wenhao, Lu, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812163/
https://www.ncbi.nlm.nih.gov/pubmed/33490161
http://dx.doi.org/10.21037/atm-20-7165

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812163/
https://www.ncbi.nlm.nih.gov/pubmed/33490161
http://dx.doi.org/10.21037/atm-20-7165

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