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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:J Clin Invest
Autors principals: Refetoff, S, Fang, V S, Marshall, J S, Robin, N I
Format: Artigo
Idioma:Inglês
Publicat: American Society for Clinical Investigation 1976
Matèries:
Research Article
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars