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Study of Four New Kindreds with Inherited Thyroxine-Binding Globulin Abnormalities POSSIBLE MUTATIONS OF A SINGLE GENE LOCUS

Five families with inherited thyroxine-binding globulin (TBG) abnormalities were studied. On the basis of serum thyroxine (T(4))- binding capacity of TBG in affected males, three family types were identified: TBG deficiency, low TBG, and high TBG capacity. In all families evidence for X-linked inher...

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Bibliografiske detaljer
Udgivet i:J Clin Invest
Main Authors: Refetoff, Samuel, Robin, Noel I., Alper, Chester A.
Format: Artigo
Sprog:Inglês
Udgivet: American Society for Clinical Investigation 1972
Fag:
Online adgang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC302199/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/4111366/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI106880
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