Prospects of Zinc Supplementation in Autism Spectrum Disorders and Shankopathies Such as Phelan McDermid Syndrome

The loss of one copy of SHANK3 (SH3 and multiple ankyrin repeat domains 3) in humans highly contributes to Phelan McDermid syndrome (PMDS). In addition, SHANK3 was identified as a major autism candidate gene. Interestingly, the protein encoded by the SHANK3 gene is regulated by zinc. While zinc defi...

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Detalles Bibliográficos
Autores principales: Hagmeyer, Simone, Sauer, Ann Katrin, Grabrucker, Andreas M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974951/
https://www.ncbi.nlm.nih.gov/pubmed/29875651
http://dx.doi.org/10.3389/fnsyn.2018.00011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974951/
https://www.ncbi.nlm.nih.gov/pubmed/29875651
http://dx.doi.org/10.3389/fnsyn.2018.00011

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