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Corrigendum to molecular genetics and emerging therapies for retinitis pigmentosa: Basic research and clinical perspective progress in retinal and eye research (2018) Vol 63,107-131.

  • Author(s): Dias, Marina França
  • Joo, Kwangsic
  • Kemp, Jessica A
  • Fialho, Silvia Ligório
  • da Silva Cunha, Armando
  • Woo, Se Joon
  • Kwon, Young Jik
  • et al.

Published Web Location

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6141772/
No data is associated with this publication.
Abstract

© 2018 The authors would like to report an error in Fig 4 where RP1 in the originally published figure should have been RP2 as in the corrected figure below. [Figure presented] Fig. 4. Causative genes and their relative proportions in Retinitis Pigmentosa (RP). The inheritance of RP consists of autosomal dominant (ad), autosomal recessive (ar), X-linked (xl) and unknown patterns. The causative genes for adRP are Rho, RPRF, PRPH2, RP1, IMPDH1 and PRPF8; for arRP, USH2A, ABCA4, PDE6A, and PDE6B and RPE65; for xlRP, RPGR and RP2. The authors would like to apologize for any inconvenience caused.

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