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Journal of Ophthalmology
Volume 2017, Article ID 3080245, 10 pages
Research Article

Genotype-Phenotype Characterization of Novel Variants in Six Italian Patients with Familial Exudative Vitreoretinopathy

1Department of Ophthalmology, Bambino Gesù IRCCS Children's Hospital, Rome, Italy
2MAGI-Human Medical Genetics Institute, Bolzano, Italy
3MAGI-Human Medical Genetics Institute, Rovereto, Italy
4Eye Clinic, Department of Neurosciences, Biomedicine and Movement, University and AOUI (Azienda Ospedaliera Universitaria Integrata) of Verona, Verona, Italy
5Dipartimento Anestesia e Rianimazione Materno Infantile, Ospedale San Filippo Neri, Rome, Italy
6“G.B. Bietti” Foundation, IRCCS, Rome, Italy

Correspondence should be addressed to Paolo Enrico Maltese; gro.igamossa@esetlam.oloap

Received 3 April 2017; Accepted 4 June 2017; Published 5 July 2017

Academic Editor: Naheed Khan

Copyright © 2017 Giancarlo Iarossi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Citations to this Article [4 citations]

The following is the list of published articles that have cited the current article.

  • Giancarlo Iarossi, Matteo Bertelli, Paolo Enrico Maltese, Elena Gusson, Giorgio Marchini, Alice Bruson, Sabrina Benedetti, Sabrina Volpetti, Gino Catena, Luca Buzzonetti, and Lucia Ziccardi, “Corrigendum to “Genotype-Phenotype Characterization of Novel Variants in Six Italian Patients with Familial Exudative Vitreoretinopathy”,” Journal of Ophthalmology, vol. 2017, pp. 1–2, 2017. View at Publisher · View at Google Scholar
  • Yian Li, Jie Peng, Jiakai Li, Qi Zhang, Jing Li, Xiang Zhang, Ping Fei, Kaiqin She, and Peiquan Zhao, “The characteristics of digenic familial exudative vitreoretinopathy,” Graefe's Archive for Clinical and Experimental Ophthalmology, 2018. View at Publisher · View at Google Scholar
  • Shujin Li, Mu Yang, Wenjing Liu, Yuqing Liu, Lin Zhang, Xianjun Zhu, Yeming Yang, Periasamy Sundaresan, and Zhenglin Yang, “Targeted Next-Generation Sequencing Reveals Novel RP1 Mutations in Autosomal Recessive Retinitis Pigmentosa,” Genetic Testing and Molecular Biomarkers, vol. 22, no. 2, pp. 109–114, 2018. View at Publisher · View at Google Scholar
  • Lisha Yang, Jingliang Cheng, Qi Zhou, Iqra Ijaz, Hongbin Lv, Jiewen Fu, Chunli Wei, and Junjiang Fu, “A novel variant of the FZD4 gene in a Chinese family causes autosomal dominant familial exudative vitreoretinopathy,” Cellular Physiology and Biochemistry, vol. 51, no. 5, pp. 2445–2455, 2018. View at Publisher · View at Google Scholar