Novel mutations in CYP4V2 in Bietti corneoretinal crystalline dystrophy: Next-generation sequencing technology and genotype-phenotype correlations

Những quyển sách tương tự

• Identification of novel CYP4V2 gene mutations in 92 Chinese families with Bietti’s crystalline corneoretinal dystrophy
  Bằng: Meng, Xiao Hong, et al.
  Được phát hành: (2014)
• Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2
  Bằng: Li, Anren, et al.
  Được phát hành: (2004)
• Expanding the Phenotypic and Genotypic Spectrum of Bietti Crystalline Dystrophy
  Bằng: da Palma, Mariana Matioli, et al.
  Được phát hành: (2021)
• Novel CYP4V2 mutations associated with Bietti crystalline corneoretinal dystrophy in Chinese patients
  Bằng: Tian, Rong, et al.
  Được phát hành: (2015)
• Identification and population history of CYP4V2 mutations in patients with Bietti crystalline corneoretinal dystrophy
  Bằng: Jiao, Xiaodong, et al.
  Được phát hành: (2017)