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...
| Auteurs principaux: | , , , , , , |
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| Format: | Journal article |
| Langue: | English |
| Publié: |
American Medical Association (AMA)
2019
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