The Impact of Mutations in Wolframin on Psychiatric Disorders
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DOI: 10.3389/fped.2021.718132
Abstract: Wolfram Syndrome is a rare autosomal recessive disease characterized by early-onset diabetes mellitus, neurodegeneration, and psychological disorders. Mutations in the gene WFS1, coding for the protein wolframin, cause Wolfram Syndrome and are associated with bipolar… read more here.
Keywords: wfs1 mutations; psychiatric disorders; wolfram syndrome; mutations wolframin ... See more keywords