Condition: RETINITIS PIGMENTOSA 80


rs145549969 in IFT140 gene and RETINITIS PIGMENTOSA 80 PMID 26968735 2016 Nonsyndromic Retinal Dystrophy due to Bi-Allelic Mutations in the Ciliary Transport Gene IFT140.

PMID 26216056 2015 Mutations in human IFT140 cause non-syndromic retinal degeneration.

PMID 26359340 2016 The ophthalmic phenotype of IFT140-related ciliopathy ranges from isolated to syndromic congenital retinal dystrophy.

rs1441549097 in IFT140;LOC105371046 gene and RETINITIS PIGMENTOSA 80 PMID 26968735 2016 Nonsyndromic Retinal Dystrophy due to Bi-Allelic Mutations in the Ciliary Transport Gene IFT140.

PMID 26359340 2016 The ophthalmic phenotype of IFT140-related ciliopathy ranges from isolated to syndromic congenital retinal dystrophy.

PMID 26216056 2015 Mutations in human IFT140 cause non-syndromic retinal degeneration.

rs1555491448 in LOC105371046;IFT140 gene and RETINITIS PIGMENTOSA 80 PMID 26216056 2015 Mutations in human IFT140 cause non-syndromic retinal degeneration.

PMID 26968735 2016 Nonsyndromic Retinal Dystrophy due to Bi-Allelic Mutations in the Ciliary Transport Gene IFT140.

PMID 26359340 2016 The ophthalmic phenotype of IFT140-related ciliopathy ranges from isolated to syndromic congenital retinal dystrophy.