bibliographic entry 12697273 [be/12697273]
https://w3id.org/oc/corpus/be/12697273

is a
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  • Cangul, H, Aycan, Z, Kendall, M. A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism, J. Pediatr. Endocrinol. Metab, 27, 2014, 323, 327, PMID: 24127536
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