Whole-exome sequencing identifies novel mutations in genes responsible for retinitis pigmentosa in 2 nonconsanguineous Chinese families

مواد مشابهة

• Whole exome sequencing identifies a novel NRL mutation in a Chinese family with autosomal dominant retinitis pigmentosa
  بواسطة: Gao, Meng, وآخرون
  منشور في: (2016)
• Identification of a novel NRL mutation in a Chinese family with retinitis pigmentosa by whole-exome sequencing
  بواسطة: Qin, Y, وآخرون
  منشور في: (2017)
• Targeted exome capture and sequencing identifies novel PRPF31 mutations in autosomal dominant retinitis pigmentosa in Chinese families
  بواسطة: Yang, Liping, وآخرون
  منشور في: (2013)
• Whole exome sequencing identified novel CRB1 mutations in Chinese and Indian populations with autosomal recessive retinitis pigmentosa
  بواسطة: Yang, Yin, وآخرون
  منشور في: (2016)
• Application of targeted panel sequencing and whole exome sequencing for 76 Chinese families with retinitis pigmentosa
  بواسطة: Handong Dan, وآخرون
  منشور في: (2020-03-01)