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A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome.
Wu, Xing; Xie, Hai-Nan; Wu, Tong; Liu, Wei; Chen, Lan-Lam; Li, Zhao-Hui; Wang, Da-Jiang; Wang, Yi; Huang, Hou-Bin.
Afiliação
  • Wu X; Department of Ophthalmology, Chinese PLA General Hospital, Beijing 100853, P.R. China.
  • Xie HN; Department of Ophthalmology, Hainan Hospital of Chinese PLA General Hospital, Sanya, Hainan 572000, P.R. China.
  • Wu T; Department of Ophthalmology, Hainan Hospital of Chinese PLA General Hospital, Sanya, Hainan 572000, P.R. China.
  • Liu W; Department of Ophthalmology, Hainan Hospital of Chinese PLA General Hospital, Sanya, Hainan 572000, P.R. China.
  • Chen LL; Department of Ophthalmology, Hainan Hospital of Chinese PLA General Hospital, Sanya, Hainan 572000, P.R. China.
  • Li ZH; Department of Ophthalmology, Hainan Hospital of Chinese PLA General Hospital, Sanya, Hainan 572000, P.R. China.
  • Wang DJ; Department of Ophthalmology, Chinese PLA General Hospital, Beijing 100853, P.R. China.
  • Wang Y; Department of Ophthalmology, Chinese PLA General Hospital, Beijing 100853, P.R. China.
  • Huang HB; Department of Ophthalmology, Hainan Hospital of Chinese PLA General Hospital, Sanya, Hainan 572000, P.R. China.
Exp Ther Med ; 18(3): 2255-2261, 2019 Sep.
Article em En | MEDLINE | ID: mdl-31410177

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article