Mutations in a specific human serum albumin thyroxine binding site define the structural basis of familial dysalbuminemic hyperthyroxinemia (Q71245691)
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scientific article published on 01 August 1996
Language | Label | Description | Also known as |
---|---|---|---|
English | Mutations in a specific human serum albumin thyroxine binding site define the structural basis of familial dysalbuminemic hyperthyroxinemia |
scientific article published on 01 August 1996 |
Statements
Mutations in a specific human serum albumin thyroxine binding site define the structural basis of familial dysalbuminemic hyperthyroxinemia (English)
C E Petersen
C E Ha
D M Jameson
1 August 1996