Hereditary complete thyroxine-binding globulin deficiency: identification by T3 resin uptake test and DNA analysis.

Noguchi, T; Yamamori, I; Takamatsu, J; Nakajima, T; Mori, Y; Kumahara, Y

Noguchi, T; Yamamori, I; Takamatsu, J; Nakajima, T; Mori, Y; Kumahara, Y.

Affiliation

Noguchi T; Sakuragaoka Hospitel, Hyogo, Japan.

Intern Med ; 32(1): 6-9, 1993 Jan.

Article in En | MEDLINE | ID: mdl-8495048

Subject(s)

Thyroxine-Binding Proteins/deficiency; Thyroxine-Binding Proteins/genetics; DNA Mutational Analysis; Female; Genetic Linkage; Humans; Male; Middle Aged; Pedigree; Sequence Deletion; Thyroid Hormones/blood; Triiodothyronine/pharmacokinetics; X Chromosome

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Collection: 01-internacional Database: MEDLINE Main subject: Thyroxine-Binding Proteins Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Male / Middle aged Language: En Journal: Intern Med Journal subject: MEDICINA INTERNA Year: 1993 Document type: Article Affiliation country: Japan

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