The Impact of Mutations in Wolframin on Psychiatric Disorders

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 disorder and schizophrenia. This...

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Detalles Bibliográficos
Autores principales: Munshani, Saira, Ibrahim, Eiman Y., Domenicano, Ilaria, Ehrlich, Barbara E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567103/
https://www.ncbi.nlm.nih.gov/pubmed/34746052
http://dx.doi.org/10.3389/fped.2021.718132

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567103/
https://www.ncbi.nlm.nih.gov/pubmed/34746052
http://dx.doi.org/10.3389/fped.2021.718132

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