Zinc deficiency and low enterocyte zinc transporter expression in human patients with autism related mutations in SHANK3

Phelan McDermid Syndrome (PMDS) is a genetic disorder characterized by features of Autism spectrum disorders. Similar to reports of Zn deficiency in autistic children, we have previously reported high incidence of Zn deficiency in PMDS. However, the underlying mechanisms are currently not well under...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Sci Rep
Päätekijät: Pfaender, Stefanie, Sauer, Ann Katrin, Hagmeyer, Simone, Mangus, Katharina, Linta, Leonhard, Liebau, Stefan, Bockmann, Juergen, Huguet, Guillaume, Bourgeron, Thomas, Boeckers, Tobias M., Grabrucker, Andreas M.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Nature Publishing Group 2017
Aiheet:
Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5366950/
https://ncbi.nlm.nih.gov/pubmed/28345660
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep45190
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