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Results 1 - 6 of 6 for "X-linked" "cone-rod" dystrophy 1
  1. ... Testing Registry: Cone-rod dystrophy Genetic Testing Registry: X-linked cone-rod dystrophy 1 Genetic Testing Registry: X-linked cone-rod dystrophy ... CONE-ROD DYSTROPHY 6; CORD6 CONE-ROD DYSTROPHY, X-LINKED, 1; CORDX1 CONE-ROD DYSTROPHY 5; CORD5 CONE-ROD DYSTROPHY, X-LINKED, 2; ...
  2. ... WITHOUT DEAFNESS; RPSRDF RETINITIS PIGMENTOSA GTPase REGULATOR; RPGR CONE-ROD DYSTROPHY, X-LINKED, 1; CORDX1 NCBI Gene ClinVar Ayyagari R, Demirci FY, ...
  3. ... least one other CACNA1F mutation is responsible for X-linked cone-rod ... of the alpha-1 subunit, which likely prevents the production of functional ...
  4. ... the primary cilium. Hum Mol Genet. 2010 Apr 1;19(7):1358-67. doi: ... X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the ...
  5. ... and RP2 genes account for most cases of X-linked retinitis pigmentosa.The genes associated with retinitis pigmentosa play essential ... an X-linked pattern. The genes associated with X-linked retinitis pigmentosa are located on the X chromosome, which is ...
  6. ... ClinicalTrials.gov MYOPIA 2, AUTOSOMAL DOMINANT; MYP2 MYOPIA 1, X-LINKED; MYP1 MYOPIA 13, X-LINKED; MYP13 MYOPIA 18, ...