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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Int J Mol Sci
Egile Nagusiak: Benthani, Fahad, Tran, Phuong N., Currey, Nicola, Ng, Irvin, Giry-Laterriere, Marc, Carey, Louise, Kohonen-Corish, Maija R. J., Pangon, Laurent
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: MDPI 2015
Gaiak:
Brief Report
Sarrera elektronikoa: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
Etiketak: Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!

Antzeko izenburuak