Commentary on "Exome sequencing and electro-clinical features in pediatric patients with very early-onset retinal dystrophies: A cohort study"

Eur J Paediatr Neurol. 2021 Mar:31:106-107. doi: 10.1016/j.ejpn.2021.03.004. Epub 2021 Mar 8.

Authors

Kimia Heydari¹, Sarah R Levi¹, Stephen H Tsang²

Affiliations

¹ Jonas Children's Vision Care, Department of Ophthalmology, New York-Presbyterian Hospital, New York, NY, USA.
² Jonas Children's Vision Care, Department of Ophthalmology, New York-Presbyterian Hospital, New York, NY, USA; Department of Pathology & Cell Biology, Institute of Human Nutrition, and Columbia Stem Cell Initiative, New York, NY, USA. Electronic address: [email protected].

PMID: 33736886
DOI: 10.1016/j.ejpn.2021.03.004

No abstract available

Publication types

Editorial
Comment

MeSH terms

Child
Cohort Studies
Exome Sequencing
Exome*
Humans
Retinal Dystrophies* / diagnosis
Retinal Dystrophies* / genetics