First Report of Familial Dysalbuminemic Hyperthyroxinemia With an ALB Variant

Familial dysalbuminemic hyperthyroxinemia (FDH) is an inherited disease characterized by increased circulating total thyroxine (T4) levels and normal physiological thyroid function. Heterozygous albumin gene (ALB) variants have been reported to be the underlying cause of FDH. To our knowledge, there...

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Bibliografski detalji
Izdano u:Ann Lab Med
Glavni autori: Cho, Yoon Young, Song, Ju-Sun, Park, Hyung-Doo, Kim, Young Nam, Kim, Hye-In, Kim, Tae Hyuk, Chung, Jae Hoon, Ki, Chang-Seok, Kim, Sun Wook
Format: Artigo
Jezik:Inglês
Izdano: The Korean Society for Laboratory Medicine 2017
Teme:
Case Report
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5107620/
https://ncbi.nlm.nih.gov/pubmed/27834068
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3343/alm.2017.37.1.63
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