Correction to: Clinical and genetic characteristics of 14 patients from 13 Japanese families with RPGR-associated retinal disorder: report of eight novel variants

Podobne knjige/članki

• Clinical and genetic characteristics of 14 patients from 13 Japanese families with RPGR-associated retinal disorder: report of eight novel variants
  od: Mawatari, Go, et al.
  Izdano: (2019)
• Clinical findings of end-stage retinitis pigmentosa with a homozygous PDE6A variant (p.R653X)
  od: Mizobuchi, Kei, et al.
  Izdano: (2018)
• Characterization of GUCA1A-associated dominant cone/cone-rod dystrophy: low prevalence among Japanese patients with inherited retinal dystrophies
  od: Mizobuchi, Kei, et al.
  Izdano: (2019)
• Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency
  od: Yang, Lizhu, et al.
  Izdano: (2020)
• Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association
  od: Fujinami-Yokokawa, Yu, et al.
  Izdano: (2020)