Founder mutations of CYP1B1 gene in patients with congenital glaucoma from the United States and Brazil

Documenti analoghi

• CYP1B1, MYOC, and LTBP2 Mutations in Primary Congenital Glaucoma Patients in the United States
  di: LIM, SING-HUI, et al.
  Pubblicazione: (2012)
• CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma
  di: Coêlho, Rodrigo E.A., et al.
  Pubblicazione: (2019)
• Investigation of CYP1B1 mutations in Chinese patients with primary congenital glaucoma
  di: Yang, Mei, et al.
  Pubblicazione: (2009)
• Mutation spectrum of CYP1B1 in North Indian congenital glaucoma patients
  di: Tanwar, Mukesh, et al.
  Pubblicazione: (2009)
• Analysis of CYP1B1 Gene Mutations in Patients with Primary Congenital Glaucoma
  di: Chouiter, Leila, et al.
  Pubblicazione: (2017)