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Publications by SL Fang

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

European Journal of Endocrinology

English

Related publications

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

Journal of Biological Chemistry

English

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

Oncotarget

Oncology

2015

English

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

Lipids in Health and Disease

Biochemistry

Endocrinology

Clinical Biochemistry

Metabolism

Diabetes

2016

English

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)

English

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

Journal of Human Genetics

Genetics

2001

English

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

Tohoku Journal of Experimental Medicine

English

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

Frontiers in Medicine

Medicine

2019

English

A Novel POLG Gene Mutation in a Patient With SANDO

Journal of Experimental and Integrative Medicine

Alternative Medicine

Complementary

2012

English

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

Molecular genetics & genomic medicine

Genetics

Molecular Biology

2019

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by SL Fang

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

Related publications

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