Novel mutations of CRB1 in Chinese families presenting with retinal dystrophies

Lignende værker

• Targeted exome capture and sequencing identifies novel PRPF31 mutations in autosomal dominant retinitis pigmentosa in Chinese families
  af: Yang, Liping, et al.
  Udgivet: (2013)
• Novel Mutations of RPGR in Chinese Retinitis Pigmentosa Patients and the Genotype-Phenotype Correlation
  af: Yang, Liping, et al.
  Udgivet: (2014)
• Application of Whole Exome and Targeted Panel Sequencing in the Clinical Molecular Diagnosis of 319 Chinese Families with Inherited Retinal Dystrophy and Comparison Study
  af: Wang, Likun, et al.
  Udgivet: (2018)
• CRB1 mutations in inherited retinal dystrophies
  af: Bujakowska, Kinga, et al.
  Udgivet: (2011)
• Novel mutations of RPGR in Chinese families with X-linked retinitis pigmentosa
  af: Zhang, Zhimeng, et al.
  Udgivet: (2019)