RP38 |
RP105 |
KSHV ORF73 |
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[Retinitis pigmentosa 41] This term refers to a retinal dystrophy, which is characterized by retinal pigment deposits and the primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors and is due to mutations in the gene encoding CD133 (prominin-1) (Maw et al, 2000; Zhang et al, 2007).
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