Clinical characterization of retinitis pigmentosa associated with variants in SNRNP200

<p><strong>Importance</strong>&nbsp;&nbsp;<em>SNRNP200</em>&nbsp;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...

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Bibliographic Details
Main Authors: Yusuf, IH, Birtel, J, Shanks, ME, Clouston, P, Downes, SM, Charbel Issa, P, MacLaren, RE
Format: Journal article
Language:English
Published: American Medical Association (AMA) 2019