- DUOX2 Mutations Are Frequently Associated With Congenital Hypothyroidism in the Korean Population
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Park KJ, Park HK, Kim YJ, Lee KR, Park JH, Park JH, Park HD, Lee SY, Kim JW
- KMID: 2373514
- Ann Lab Med.
- 2016 Mar;36(2):145-153.
- doi: 10.3343/alm.2016.36.2.145
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... -
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