Familial dysalbuminemic hyperthyroxinemia in a 12‐year‐old girl
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DOI: 10.1111/ped.13839
Abstract: 1 Lehnhardt A, Karnatz C, Ahlenstiel-Grunow T et al. Clinical and molecular characterization of patients with heterozygous mutations in Wilms tumor suppressor gene 1. Clin. J. Am. Soc. Nephrol. 2015; 10: 825–31. 2 Nagatani K,… read more here.
Keywords: familial dysalbuminemic; old girl; hyperthyroxinemia year; soc nephrol ... See more keywords