Back to search

Article

Retinoschisis and Norrie Disease: A missing link

2021-03-18

Abstract excerpt

<title>Abstract</title> <p>Objective: Retinoschisis and Norrie disease are X-linked recessive retinal disorders caused by mutations in RS1 and NDP genes respectively. Both are likely to be monogenic and no locus heterogeneity has been reported. However, there are reports showing overlapping features of Norrie disease and retinoschisis in a NDP knock-out mouse model and also the involvement of both the genes in re...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
ca5186c0-d1cf-5171-8853-2e18e7675daf
DOI
10.21203/rs.3.rs-322315/v1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Retinoschisis and Norrie Disease: A missing linkDOI 10.21203/rs.3.rs-322315/v1
Select a neighboring publication to make it the new centre.