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

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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Bibliographic Details
Main Authors: Qingping Zhang, Jiaping Wang, Jiarui Li, Xinhua Bao, Ying Zhao, Xiaoying Zhang, Liping Wei, Xiru Wu
Format: Article
Language:English
Published: BMC 2017-08-01
Series:BMC Medical Genetics
Subjects:
FOXG1
RTT
RTT-like MR
Epilepsy
Hypoplasia of corpus callosum
Online Access:http://link.springer.com/article/10.1186/s12881-017-0455-y

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http://link.springer.com/article/10.1186/s12881-017-0455-y

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