Clinical characterization of retinitis pigmentosa associated with variants in SNRNP200
<p><strong>Importance</strong> <em>SNRNP200</em> is a recently identified genetic cause of autosomal dominant retinitis pigmentosa (RP). However, the associated retinal phenotype is not well characterized.</p> <p><strong>Obj...
Prif Awduron: | , , , , , , |
---|---|
Fformat: | Journal article |
Iaith: | English |
Cyhoeddwyd: |
American Medical Association (AMA)
2019
|