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...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Pubblicato in:Int J Mol Sci
Autori principali: Benthani, Fahad, Tran, Phuong N., Currey, Nicola, Ng, Irvin, Giry-Laterriere, Marc, Carey, Louise, Kohonen-Corish, Maija R. J., Pangon, Laurent
Natura: Artigo
Lingua:Inglês
Pubblicazione: MDPI 2015
Soggetti:
Brief Report
Accesso online: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
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi