Response to Finsterer’s “Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome”

Julia Chertkofa Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA

Robert B. Hufnagela Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA

Delphine Blaina Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA

Andrea L. Gropmanb Department of Neurology, Children’s National Medical Center, Washington, District of Columbia, USA

Brian P. Brooksa Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USACorrespondence[email protected]

https://orcid.org/0000-0002-1916-7551

"Response to Finsterer’s “Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome”." Ophthalmic Genetics, 42(1), p. 100

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The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article.

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Response to Finsterer’s “Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome”

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Response to Finsterer’s “Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome”

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