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Cone rod dystrophies.
Hamel CP
Orphanet J Rare Dis
2007,
2
:7
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PubMed Central articles that cite the above article:
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Unexpected novel relational links uncovered by extensive developmental profiling of nuclear receptor expression.
Bertrand S, Thisse B, Tavares R, Sachs L, Chaumot A, Bardet PL, Escrivà H, Duffraisse M, Marchand O, Safi R, Thisse C, Laudet V
PLoS Genet
2007 Nov,
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ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies.
Kitiratschky VB, Grau T, Bernd A, Zrenner E, Jägle H, Renner AB, Kellner U, Rudolph G, Jacobson SG, Cideciyan AV, Schaich S, Kohl S, Wissinger B
Eur J Hum Genet
2008 Jul,
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A novel GCAP1(N104K) mutation in EF-hand 3 (EF3) linked to autosomal dominant cone dystrophy.
Jiang L, Wheaton D, Bereta G, Zhang K, Palczewski K, Birch DG, Baehr W
Vision Res
2008 Oct,
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Mutations in CNNM4 cause recessive cone-rod dystrophy with amelogenesis imperfecta.
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CLRN1 is nonessential in the mouse retina but is required for cochlear hair cell development.
Geller SF, Guerin KI, Visel M, Pham A, Lee ES, Dror AA, Avraham KB, Hayashi T, Ray CA, Reh TA, Bermingham-McDonogh O, Triffo WJ, Bao S, Isosomppi J, Västinsalo H, Sankila EM, Flannery JG
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V1 projection zone signals in human macular degeneration depend on task, not stimulus.
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