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.