(PDF) R127w-HNF-4α Is a Loss of Function Mutation but Not a

R127w-HNF-4α Is a Loss of Function Mutation but Not a Rare Polymorphism and Causes Type II Diabetes in a Japanese Family With MODY1

Diabetologia - Germany

doi 10.1007/s001250051338

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April 13, 2000

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Springer Science and Business Media LLC

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R127w-HNF-4α Is a Loss of Function Mutation but Not a Rare Polymorphism and Causes Type II Diabetes in a Japanese Family With MODY1

Diabetologia - Germany

doi 10.1007/s001250051338

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

T130I Mutation in HNF-4α Gene Is a Loss-Of-Function Mutation in Hepatocytes and Is Associated With Late-Onset Type 2 Diabetes Mellitus in Japanese Subjects

Loss-Of-Function Mutation in Thiamine Transporter 1 in a Family With Autosomal Dominant Diabetes

Rare Variants Identified in the HNF-4α Β-Cell-Specific Promoter and Alternative Exon 1 Lack Biological Significance in Maturity Onset Diabetes of the Young and Young Onset Type II Diabetes

A Family History of Diabetes Is Not Associated With Arterial Stiffness in Non-Diabetic Japanese Population

A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family

Mild Cone‐rod Dystrophy and Sensorineural Hearing Loss With CEP250 Mutation in a Japanese Family

UBR5Gene Mutation Is Associated With Familial Adult Myoclonic Epilepsy in a Japanese Family

Trp64Arg Polymorphism of the Beta3-Adrenergic Receptor Is Not Associated With Diabetic Nephropathy in Japanese Patients With Type 2 Diabetes

A Mutation in MT-TW Causes a tRNA Processing Defect and Reduced Mitochondrial Function in a Family With Leigh Syndrome