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pubmed-article:2946372pubmed:abstractTextTwo kinds of TBG polymorphism are described in human, one found in deglycosylated TBG from individual blood donors, the other is a genetically determined polymorphism. TBG from plasma samples from a patient with toxic goiter, not autoimmune, (p)TBG, from the patient's mother (m)TBG and from individual donors (n)TBG, were labeled with [125I]T4 or [125I]T3 and submitted to isoelectric focusing (IEF), followed by autoradiography. Three faint [125I]T4 radiolabeled bands were detectable in (p)TBG while four strong [125I]T4 radiolabeled bands were detectable in (m)TBG and (n)TBG), respectively. IEF of the [125I]T3 incubated serum samples resulted in no detectable isoelectric radiolabeled band for (p)TBG while a normal pattern was found in (m)TBG and in (n)TBG, respectively. These data suggest a new intraindividual not linked to sexual chromosome X polymorphism characterized by a loss in hormone binding.lld:pubmed
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pubmed-article:2946372pubmed:pagination277-83lld:pubmed
pubmed-article:2946372pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:2946372pubmed:year1986lld:pubmed
pubmed-article:2946372pubmed:articleTitle[Polymorphism of human thyroxine binding serum globulin (TBG); existence of a new form of serum protein without detectable triiodothyronine binding power].lld:pubmed
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pubmed-article:2946372pubmed:publicationTypeEnglish Abstractlld:pubmed