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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Bibliografiska uppgifter
I publikationen:Ann Lab Med
Huvudupphovsmän: 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
Materialtyp: Artigo
Språk:Inglês
Publicerad: The Korean Society for Laboratory Medicine 2016
Ämnen:
Original Article
Länkar: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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