Response to Finsterer's "Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome"
Ophthalmic Genet
.
2021 Feb;42(1):100.
doi: 10.1080/13816810.2020.1832295.
Epub 2020 Nov 24.
Authors
Julia Chertkof
1
,
Robert B Hufnagel
1
,
Delphine Blain
1
,
Andrea L Gropman
2
,
Brian P Brooks
1
Affiliations
1
Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health , Bethesda, Maryland, USA.
2
Department of Neurology, Children's National Medical Center , Washington, District of Columbia, USA.
PMID:
33233984
PMCID:
PMC8127728
DOI:
10.1080/13816810.2020.1832295
No abstract available
Publication types
Letter
Comment
MeSH terms
Humans
Kearns-Sayre Syndrome*
Retinoschisis* / diagnosis
Retinoschisis* / genetics
Grants and funding
ZIA EY000564/ImNIH/Intramural NIH HHS/United States