Cited by

• Clinical and Genetic Characteristics of 15 Affected Patients From 12 Japanese Families with GUCY2D-Associated Retinal Disorder.

  Liu X, Fujinami K, Kuniyoshi K, Kondo M, Ueno S, Hayashi T, Mochizuki K, Kameya S, Yang L, Fujinami-Yokokawa Y, Arno G, Pontikos N, Sakuramoto H, Kominami T, Terasaki H, Katagiri S, Mizobuchi K, Nakamura N, Yoshitake K, Miyake Y, Li S, Kurihara T, Tsubota K, Iwata T, Tsunoda K; Japan Eye Genetics Consortium. Liu X, et al. Transl Vis Sci Technol. 2020 May 11;9(6):2. doi: 10.1167/tvst.9.6.2. eCollection 2020 May. Transl Vis Sci Technol. 2020. PMID: 32821499 Free PMC article.
• GUCY2D-Related Retinal Dystrophy with Autosomal Dominant Inheritance-A Multicenter Case Series and Review of Reported Data.

  Neubauer J, Hahn L, Birtel J, Boon CJF, Charbel Issa P, Fischer MD. Neubauer J, et al. Genes (Basel). 2022 Feb 8;13(2):313. doi: 10.3390/genes13020313. Genes (Basel). 2022. PMID: 35205358 Free PMC article.
• A detailed phenotypic description of autosomal dominant cone dystrophy due to a de novo mutation in the GUCY2D gene.

  Mukherjee R, Robson AG, Holder GE, Stockman A, Egan CA, Moore AT, Webster AR. Mukherjee R, et al. Eye (Lond). 2014 Apr;28(4):481-7. doi: 10.1038/eye.2014.7. Epub 2014 Jan 31. Eye (Lond). 2014. PMID: 24480840 Free PMC article.
• Disease progression in autosomal dominant cone-rod dystrophy caused by a novel mutation (D100G) in the GUCA1A gene.

  Nong E, Lee W, Merriam JE, Allikmets R, Tsang SH. Nong E, et al. Doc Ophthalmol. 2014 Feb;128(1):59-67. doi: 10.1007/s10633-013-9420-z. Epub 2013 Dec 19. Doc Ophthalmol. 2014. PMID: 24352742 Free PMC article.
• Genome editing in large animal models.

  Maynard LH, Humbert O, Peterson CW, Kiem HP. Maynard LH, et al. Mol Ther. 2021 Nov 3;29(11):3140-3152. doi: 10.1016/j.ymthe.2021.09.026. Epub 2021 Oct 1. Mol Ther. 2021. PMID: 34601132 Free PMC article. Review.