Iodide transport defect: functional characterization of a novel mutation in the Na+/I- symporter 5'-untranslated region in a patient with congenital hypothyroidism

NICOLA, JP; NAZAR, M; SERRANO-NASCIMENTO, C; GOULART-SILVA, F; SOBRERO, G; TESTA, G; NUNEZ, MT; MUÑOZ, L; MIRAS, M; MASINI-REPISO, AM

ENDOCRINE SOC

Año: 2011 vol. 96 p. 1100 - 1100

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