DUOX2 Mutations Are Frequently Associated With Congenital Hypothyroidism in the Korean Population

BACKGROUND: Most cases with congenital hypothyroidism (CH) are usually sporadic, while about 20% of the cases are caused by genetic defects. Little information is available regarding the mutation incidence and genetic heterogeneity of CH in Koreans. We aimed to determine the mutation incidence of CH...

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Detalles Bibliográficos
Autores principales: Park, Kyoung-Jin, Park, Hyun-Kyung, Kim, Young-Jin, Lee, Kyoung-Ryul, Park, Jong-Ho, Park, June-Hee, Park, Hyung-Doo, Lee, Soo-Youn, Kim, Jong-Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Laboratory Medicine 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4713848/
https://www.ncbi.nlm.nih.gov/pubmed/26709262
http://dx.doi.org/10.3343/alm.2016.36.2.145

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4713848/
https://www.ncbi.nlm.nih.gov/pubmed/26709262
http://dx.doi.org/10.3343/alm.2016.36.2.145

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