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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

Genetic DeterminantMendelian DisorderMissense VariationsGenetic DisorderGeneticsInherited Metabolic DiseaseDiabetesPathologyArg456his MutationMolecular GeneticsWolfram SyndromeDisease Gene IdentificationMedicine