FOXP2 promotes the nuclear translocation of POT1, but FOXP2(R553H), mutation related to speech-language disorder, partially prevents it

✍ Scribed by Yuko Tanabe; Eriko Fujita; Takashi Momoi

• Book ID: 116301940
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 503 KB
• Volume: 410
• Category: Article
• ISSN: 0006-291X
• DOI: 10.1016/j.bbrc.2011.06.032