Your browser doesn't support javascript.
loading
A novel tandem duplication of PRDM13 in a Chinese family with North Carolina macular dystrophy.
Wu, Shijing; Yuan, Zhisheng; Sun, Zixi; Zhu, Tian; Wei, Xing; Zou, Xuan; Sui, Ruifang.
Affiliation
  • Wu S; Department of Ophthalmology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
  • Yuan Z; Department of Ophthalmology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
  • Sun Z; Department of Ophthalmology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
  • Zhu T; Department of Ophthalmology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
  • Wei X; Department of Ophthalmology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
  • Zou X; Department of Ophthalmology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
  • Sui R; Department of Ophthalmology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China. hrfsui@163.com.
Graefes Arch Clin Exp Ophthalmol ; 260(2): 645-653, 2022 Feb.
Article in En | MEDLINE | ID: mdl-34427740
Subject(s)
Key words
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Database: MEDLINE Main subject: Corneal Dystrophies, Hereditary Limits: Humans Country/Region as subject: Asia Language: En Journal: Graefes Arch Clin Exp Ophthalmol Year: 2022 Type: Article Affiliation country: China
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Database: MEDLINE Main subject: Corneal Dystrophies, Hereditary Limits: Humans Country/Region as subject: Asia Language: En Journal: Graefes Arch Clin Exp Ophthalmol Year: 2022 Type: Article Affiliation country: China