bibliographic entry 12697277 [be/12697277]
https://w3id.org/oc/corpus/be/12697277
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Satoh, M, Aso, K, Ogikubo, S. Hypothyroidism caused by the combination of two heterozygous mutations: one in the TSH receptor gene the other in the DUOX2 gene, J. Pediatr. Endocrinol. Metab, 28, 2015, 657, 661, PMID: 25928756
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