Concepedia

Missense Variations of the Gene Responsible for Wolfram Syndrome (WFS1/wolframin) in Japanese: Possible Contribution of the Arg456His Mutation to Type 1 Diabetes as a Nonautoimmune Genetic Basis

Takuya Awata, Kiyoaki Inoue, Susumu Kurihara, Tomoko Ohkubo, Ikuo Inoue, Takahiro Abe, Hirofumi Takino, Yasunori Kanazawa, Shigehiro Katayama

Biochemical and Biophysical Research Communications · 2000 · 46 citations · 15 references

DOI

Concepts

References

15

Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus

Diabetes Care · 1997 · 6.2K citations

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A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)

Hiroshi Inoue, Yukio Tanizawa, P Behn et al. · Nature Genetics · 1998 · 755 citations

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Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome

Timothy Barrett, Sarah Bundey, A F Macleod · The Lancet · 1995 · 636 citations

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Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein

Tim M. Strom · Human Molecular Genetics · 1998 · 482 citations · Full text

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Clinical and Molecular Genetic Analysis of 19 Wolfram Syndrome Kindreds Demonstrating a Wide Spectrum of Mutations in WFS1

Carol Hardy, Farhat L. Khanim, Rosarelis Torres et al. · The American Journal of Human Genetics · 1999 · 217 citations · Full text

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