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Clinical and genetic characterization of a large cohort of Chinese patients with Bietti crystalline retinopathy.
Li, Huajin; Wei, Xing; Wu, Shijing; Zhu, Tian; Sun, Zixi; Li, Hui; Han, Xiaoxu; Zou, Xuan; Yao, Fengxia; Sui, Ruifang.
Affiliation
  • Li H; Department of Ophthalmology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
  • Wei X; Department of Ophthalmology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
  • Wu S; Department of Ophthalmology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
  • Zhu T; State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
  • Sun Z; Department of Ophthalmology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
  • Li H; Department of Ophthalmology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
  • Han X; Department of Ophthalmology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
  • Zou X; State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
  • Yao F; Department of Ophthalmology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
  • Sui R; Department of Ophthalmology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
Graefes Arch Clin Exp Ophthalmol ; 262(1): 337-351, 2024 Jan.
Article in En | MEDLINE | ID: mdl-37584790
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Full text: 1 Database: MEDLINE Main subject: Retinal Diseases / Corneal Dystrophies, Hereditary / Cytochrome P450 Family 4 Limits: Adult / Humans Country/Region as subject: Asia Language: En Journal: Graefes Arch Clin Exp Ophthalmol Year: 2024 Type: Article Affiliation country: China
Fulltext
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Full text: 1 Database: MEDLINE Main subject: Retinal Diseases / Corneal Dystrophies, Hereditary / Cytochrome P450 Family 4 Limits: Adult / Humans Country/Region as subject: Asia Language: En Journal: Graefes Arch Clin Exp Ophthalmol Year: 2024 Type: Article Affiliation country: China