Response to Finsterer's "Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome"
- PMID: 33233984
- PMCID: PMC8127728
- DOI: 10.1080/13816810.2020.1832295
Response to Finsterer's "Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome"
Conflict of interest statement
Declaration of interest
The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article.
Comment on
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Retinoschisis associated with Kearns-Sayre syndrome.Ophthalmic Genet. 2020 Oct;41(5):497-500. doi: 10.1080/13816810.2020.1799416. Epub 2020 Aug 13. Ophthalmic Genet. 2020. PMID: 32787478 Free PMC article.
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Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome.Ophthalmic Genet. 2021 Feb;42(1):99. doi: 10.1080/13816810.2020.1827444. Epub 2020 Sep 25. Ophthalmic Genet. 2021. PMID: 32975160 No abstract available.
References
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- Stone EM, Andorf JL, Whitmore SS, DeLuca AP, Giacalone JC, Streb LM, Braun TA, Mullins RF, Scheetz TE, Sheffield VC, et al. Clinically focused molecular investigation of 1000 consecutive families with inherited retinal disease. Ophthalmology. 2017;124 (9):1314–31. doi:10.1016/j.ophtha.2017.04.008. - DOI - PMC - PubMed
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