Condition: CONE-ROD DYSTROPHY 20
rs76216585
in
POC1B
gene and
CONE-ROD DYSTROPHY 20
PMID 25044745
2014 Mutation of POC1B in a severe syndromic retinal ciliopathy.
PMID 24945461
2014 Novel recessive cone-rod dystrophy caused by POC1B mutation.
PMID 25018096
2014 Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy.