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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Detalhes bibliográficos
Publicado no:Ann Lab Med
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: The Korean Society for Laboratory Medicine 2016
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4713848/
https://ncbi.nlm.nih.gov/pubmed/26709262
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3343/alm.2016.36.2.145
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