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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Dades bibliogràfiques
Publicat a:Int J Mol Sci
Autors principals: Benthani, Fahad, Tran, Phuong N., Currey, Nicola, Ng, Irvin, Giry-Laterriere, Marc, Carey, Louise, Kohonen-Corish, Maija R. J., Pangon, Laurent
Format: Artigo
Idioma:Inglês
Publicat: MDPI 2015
Matèries:
Brief Report
Accés en línia: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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