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

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 were ide...

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Detalles Bibliográficos
Autores principales: Zhang, Qingping, Wang, Jiaping, Li, Jiarui, Bao, Xinhua, Zhao, Ying, Zhang, Xiaoying, Wei, Liping, Wu, Xiru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575846/
https://www.ncbi.nlm.nih.gov/pubmed/28851325
http://dx.doi.org/10.1186/s12881-017-0455-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575846/
https://www.ncbi.nlm.nih.gov/pubmed/28851325
http://dx.doi.org/10.1186/s12881-017-0455-y

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