Response to Finsterer's "Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome".

Authors

Julia Chertkof
Robert B Hufnagel
Delphine Blain
Andrea L. Gropman, George Washington University
Brian P Brooks

Document Type

Journal Article

Publication Date

2-1-2021

Journal

Ophthalmic Genetics

Volume

42

Issue

1

Inclusive Pages

100

DOI

10.1080/13816810.2020.1832295

Keywords

Humans; Kearns-Sayre Syndrome; Retinoschisis

Comments

Epub 2020 Nov 24

APA Citation

Chertkof, J., Hufnagel, R., Blain, D., Gropman, A. L., & Brooks, B. (2021). Response to Finsterer's "Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome".. Ophthalmic Genetics, 42 (1). http://dx.doi.org/10.1080/13816810.2020.1832295

Peer Reviewed

1