bibliographic entry 12697279 [be/12697279]
https://w3id.org/oc/corpus/be/12697279

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  • Liu, S, Liu, L, Niu, X. A novel missense mutation (I26M) in DUOXA2 causing congenital goiter hypothyroidism impairs NADPH oxidase activity but not protein expression, J. Clin. Endocrinol. Metab, 100, 2015, 1225, 1229, jc20143964, PMID: 25675383
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