Novel mutations of CRB1 in Chinese families presenting with retinal dystrophies

Những quyển sách tương tự

• Targeted exome capture and sequencing identifies novel PRPF31 mutations in autosomal dominant retinitis pigmentosa in Chinese families
  Bằng: Yang, Liping, et al.
  Được phát hành: (2013)
• Novel Mutations of RPGR in Chinese Retinitis Pigmentosa Patients and the Genotype-Phenotype Correlation
  Bằng: Yang, Liping, et al.
  Được phát hành: (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
  Bằng: Wang, Likun, et al.
  Được phát hành: (2018)
• Novel mutations of RPGR in Chinese families with X-linked retinitis pigmentosa
  Bằng: Zhang, Zhimeng, et al.
  Được phát hành: (2019)
• CRB1 mutations in inherited retinal dystrophies
  Bằng: Bujakowska, Kinga, et al.
  Được phát hành: (2011)