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A 69 kb Deletion in chr19q13.42 including PRPF31 Gene in a Chinese Family Affected with Autosomal Dominant Retinitis Pigmentosa.
Lan, Yuanzheng; Chen, Yuhong; Qiao, Yunsheng; Xu, Qingdan; Zhai, Ruyi; Sun, Xinghuai; Wu, Jihong; Chen, Xueli.
Afiliação
  • Lan Y; Department of Ophthalmology, Eye and ENT Hospital, Fudan University, Shanghai 200031, China.
  • Chen Y; Department of Ophthalmology, Eye and ENT Hospital, Fudan University, Shanghai 200031, China.
  • Qiao Y; NHC Key Laboratory of Myopia, Chinese Academy of Medical Sciences, Fudan University, Shanghai 200031, China.
  • Xu Q; Shanghai Key Laboratory of Visual Impairment and Restoration, Shanghai 200031, China.
  • Zhai R; Department of Ophthalmology, Eye and ENT Hospital, Fudan University, Shanghai 200031, China.
  • Sun X; Department of Ophthalmology, Eye and ENT Hospital, Fudan University, Shanghai 200031, China.
  • Wu J; Department of Ophthalmology, Eye and ENT Hospital, Fudan University, Shanghai 200031, China.
  • Chen X; NHC Key Laboratory of Myopia, Chinese Academy of Medical Sciences, Fudan University, Shanghai 200031, China.
J Clin Med ; 11(22)2022 Nov 11.
Article em En | MEDLINE | ID: mdl-36431159
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article