X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin gene.
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Advances in understanding the molecular basis of the first steps in color visionAdaptive optics retinal imaging--clinical opportunities and challengesCuring color blindness--mice and nonhuman primatesCone Photoreceptor Structure in Patients With X-Linked Cone Dysfunction and Red-Green Color Vision Deficiency.The Degeneration and Apoptosis Patterns of Cone Photoreceptors in rd11 Mice.
P2860
X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin gene.
description
2013 nî lūn-bûn
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2013年の論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年论文
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2013年论文
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2013年论文
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name
X-linked cone dystrophy and co ...... a hybrid L/M cone opsin gene.
@ast
X-linked cone dystrophy and co ...... a hybrid L/M cone opsin gene.
@en
type
label
X-linked cone dystrophy and co ...... a hybrid L/M cone opsin gene.
@ast
X-linked cone dystrophy and co ...... a hybrid L/M cone opsin gene.
@en
prefLabel
X-linked cone dystrophy and co ...... a hybrid L/M cone opsin gene.
@ast
X-linked cone dystrophy and co ...... a hybrid L/M cone opsin gene.
@en
P2093
P2860
P50
P1433
P1476
X-linked cone dystrophy and co ...... a hybrid L/M cone opsin gene.
@en
P2093
Anthony T Moore
Joseph Carroll
Jungtae Rha
Maureen Neitz
Michel Michaelides
Michelle McClements
P2860
P356
10.1016/J.VISRES.2012.12.012
P577
2013-01-18T00:00:00Z