RP

Determining the functional disparty between CRB1 variants causing LCA and RP
Leveraging cutting-edge model systems to further understand CRB1-related eye disease
Nicholas Owen
Determining the functional disparty between CRB1 variants causing LCA and RP
Nonsyndromic Retinal Dystrophy due to Bi-Allelic Mutations in the Ciliary Transport Gene IFT140
Mutations in the ciliary transporter gene IFT140, usually associated with a severe syndromic ciliopathy, may also cause isolated retinal dystrophy. A series of patients with nonsyndromic retinitis pigmentosa (RP) due to IFT140 was investigated in this study…
S Hull, Nicholas Owen, F Islam, D Tracey-White, V Plagnol, AT Moore
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