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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Detalles Bibliográficos
Autores principales: Benthani, Fahad, Tran, Phuong N., Currey, Nicola, Ng, Irvin, Giry-Laterriere, Marc, Carey, Louise, Kohonen-Corish, Maija R. J., Pangon, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463715/
https://www.ncbi.nlm.nih.gov/pubmed/25997006
http://dx.doi.org/10.3390/ijms160511522

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463715/
https://www.ncbi.nlm.nih.gov/pubmed/25997006
http://dx.doi.org/10.3390/ijms160511522

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