Proteogenomic Analysis Identifies a Novel Human SHANK3 Isoform

Mutations of the SHANK3 gene have been associated with autism spectrum disorder. Individuals harboring different SHANK3 mutations display considerable heterogeneity in their cognitive impairment, likely due to the high SHANK3 transcriptional diversity. In this study, we report a novel interaction be...

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Bibliografiske detaljer
Udgivet i:Int J Mol Sci
Main Authors: Benthani, Fahad, Tran, Phuong N., Currey, Nicola, Ng, Irvin, Giry-Laterriere, Marc, Carey, Louise, Kohonen-Corish, Maija R. J., Pangon, Laurent
Format: Artigo
Sprog:Inglês
Udgivet: MDPI 2015
Fag:
Brief Report
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4463715/
https://ncbi.nlm.nih.gov/pubmed/25997006
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms160511522
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