Disease progression in autosomal dominant cone-rod dystrophy caused by a novel mutation (D100G) in the GUCA1A gene
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Allosteric communication pathways routed by Ca(2+)/Mg(2+) exchange in GCAP1 selectively switch target regulation modes.RNA interference gene therapy in dominant retinitis pigmentosa and cone-rod dystrophy mouse models caused by GCAP1 mutations.Electroretinography Reveals Difference in Cone Function between Syndromic and Nonsyndromic USH2A Patients.Cone dystrophy or macular dystrophy associated with novel autosomal dominant GUCA1A mutations.Molecular determinants of Guanylate Cyclase Activating Protein subcellular distribution in photoreceptor cells of the retina.
P2860
Disease progression in autosomal dominant cone-rod dystrophy caused by a novel mutation (D100G) in the GUCA1A gene
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 19 December 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Disease progression in autosom ...... ion (D100G) in the GUCA1A gene
@en
Disease progression in autosomal dominant cone-rod dystrophy caused by a novel mutation
@nl
type
label
Disease progression in autosom ...... ion (D100G) in the GUCA1A gene
@en
Disease progression in autosomal dominant cone-rod dystrophy caused by a novel mutation
@nl
prefLabel
Disease progression in autosom ...... ion (D100G) in the GUCA1A gene
@en
Disease progression in autosomal dominant cone-rod dystrophy caused by a novel mutation
@nl
P2093
P2860
P1476
Disease progression in autosom ...... ion (D100G) in the GUCA1A gene
@en
P2093
Joanna E Merriam
Rando Allikmets
Stephen H Tsang
Winston Lee
P2860
P2888
P356
10.1007/S10633-013-9420-Z
P577
2013-12-19T00:00:00Z