P35 – 1937 A new variant detected in GRIN2A by whole-exome sequencing in a patient with intellectual disability with intractable epilepsy

✍ Scribed by Per, H; Caglayan, AO; Canpolat, M; Bilguvar, K; Gümüş, H; Kumandas, S

• Book ID: 122651534
• Publisher: Elsevier Science
• Year: 2013
• Tongue: English
• Weight: 63 KB
• Volume: 17
• Category: Article
• ISSN: 1090-3798
• DOI: 10.1016/S1090-3798(13)70214-9