Metabolism of thyroxine-binding globulin in man. Abnormal rate of synthesis in inherited thyroxine-binding globulin deficiency and excess.

It has been previously suggested that inherited thyroxine-binding globulin (TBG) abnormalities in man may be due to mutations at a single X-chromosome-linked locus controlling TBG synthesis. However, abnormalities in TBG degradation have not been excluded. The availability of purified human TBG and...

Celý popis

Podrobná bibliografie

Vydáno v:	J Clin Invest
Hlavní autoři:	Refetoff, S, Fang, V S, Marshall, J S, Robin, N I
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	American Society for Clinical Investigation 1976
Témata:	Research Article
On-line přístup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC436674/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/56342/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI108301
Tagy:	Přidat tag Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!