Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation

• Egile Nagusiak: Qingping Zhang (Egilea), Jiaping Wang (Egilea), Jiarui Li (Egilea), Xinhua Bao (Egilea), Ying Zhao (Egilea), Xiaoying Zhang (Egilea), Liping Wei (Egilea), Xiru Wu (Egilea)
• Formatua: Liburua
• Argitaratua: BMC, 2017-08-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

Abstract Background We aimed to delineate clinical phenotypes associated with FOXG1 mutations in Chinese patients with Rett syndrome (RTT) or RTT-like mental retardation (MR). Methods Four hundred and fifty-one patients were recruited, including 418 with RTT and 33 with RTT-like MR. Gene mutations w...