(PDF) A Point Mutation in the Albumin Gene in a Chinese

A Point Mutation in the Albumin Gene in a Chinese Patient With Familial Dysalbuminemic Hyperthyroxinemia

European Journal of Endocrinology - United Kingdom

doi 10.1530/eje.0.1410374

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October 1, 1999

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Bioscientifica

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A Point Mutation in the Albumin Gene in a Chinese Patient With Familial Dysalbuminemic Hyperthyroxinemia

European Journal of Endocrinology - United Kingdom

doi 10.1530/eje.0.1410374

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Mutations in a Specific Human Serum Albumin Thyroxine Binding Site Define the Structural Basis of Familial Dysalbuminemic Hyperthyroxinemia

A Novel Pathogenic Germline Mutation in the Adenomatous Polyposis Coli Gene in a Chinese Family With Familial Adenomatous Coli

A Novel APOC2 Gene Mutation Identified in a Chinese Patient With Severe Hypertriglyceridemia and Recurrent Pancreatitis

A Case of Familial Dysalbuminemic Hyperthyroxinemia (FDH) in Japan: FDH as a Possible Differential Diagnosis of Syndrome of Inappropriate Secretion of Thyroid-Stimulating Hormone (SITSH)

A Chinese Homozygote of Familial Hypercholesterolemia: Identification of a Novel C263R Mutation in the LDL Receptor Gene

A Novel Mutation of the Ceruloplasmin Gene in a Patient With Heteroallelic Ceruloplasmin Gene Mutation (HypoCPGM)

A Novel Homozygous Truncating Mutation in LAMB2 Gene in a Chinese Uyghur Patient With Severe Phenotype Pierson Syndrome

A Novel POLG Gene Mutation in a Patient With SANDO

A Start Codon Mutation of the TSPAN12 Gene in Chinese Families Causes Clinical Heterogeneous Familial Exudative Vitreoretinopathy