Dominant cone dystrophy starting with blue cone involvement.
作者信息
Pinckers A
出版信息
Br J Ophthalmol. 1992 Feb;76(2):127. doi: 10.1136/bjo.76.2.127-a.
Abstract
摘要
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Br J Ophthalmol. 1992 Feb;76(2):127. doi: 10.1136/bjo.76.2.127-a.
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Basic phenomena in acquired colour vision deficiency.
Doc Ophthalmol. 1983 May 1;55(3):251-71. doi: 10.1007/BF00140812.
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Progressive peripheral cone dysfunction.
Am J Ophthalmol. 1988 Nov 15;106(5):557-60. doi: 10.1016/0002-9394(88)90585-5.
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An electroretinographic and molecular genetic study of X-linked cone degeneration.
Am J Ophthalmol. 1989 Nov 15;108(5):540-7. doi: 10.1016/0002-9394(89)90431-5.
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Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.常染色体显性遗传性视网膜色素变性患者视紫红质基因的突变
N Engl J Med. 1990 Nov 8;323(19):1302-7. doi: 10.1056/NEJM199011083231903.
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A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.视网膜色素变性一种类型中视紫红质基因的点突变。
Nature. 1990 Jan 25;343(6256):364-6. doi: 10.1038/343364a0.
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Br J Ophthalmol. 1991 Jun;75(6):332-6. doi: 10.1136/bjo.75.6.332.
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Peripheral cone disease.
Ophthalmologica. 1977;174(3):145-50. doi: 10.1159/000308592.
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