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

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...

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Main Authors: Qingping Zhang (Author), Jiaping Wang (Author), Jiarui Li (Author), Xinhua Bao (Author), Ying Zhao (Author), Xiaoying Zhang (Author), Liping Wei (Author), Xiru Wu (Author)
Format: Book
Published: BMC, 2017-08-01T00:00:00Z.
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