Clinical characterization of retinitis pigmentosa associated with variants in SNRNP200

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...

Podrobná bibliografie
Hlavní autoři:	Yusuf, IH, Birtel, J, Shanks, ME, Clouston, P, Downes, SM, Charbel Issa, P, MacLaren, RE
Médium:	Journal article
Jazyk:	English
Vydáno:	American Medical Association (AMA) 2019

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