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C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy.
Nat Genet. 2007 Sep;39(9):1068-70. doi: 10.1038/ng2082. Epub 2007 Jul 29.
Nat Genet. 2007.
PMID: 17660820
A new autosomal dominant vascular retinopathy syndrome.
Storimans CW, Van Schooneveld MJ, Oosterhuis JA, Bos PJ.
Storimans CW, et al.
Eur J Ophthalmol. 1991 Apr-Jun;1(2):73-8. doi: 10.1177/112067219100100204.
Eur J Ophthalmol. 1991.
PMID: 1821204
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Rieger's eye anomaly and persistent hyperplastic primary vitreous.
Storimans CW, Van Schooneveld MJ.
Storimans CW, et al.
Ophthalmic Paediatr Genet. 1989 Dec;10(4):257-62. doi: 10.3109/13816818909009880.
Ophthalmic Paediatr Genet. 1989.
PMID: 2628817
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Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon.
Terwindt GM, Haan J, Ophoff RA, Groenen SM, Storimans CW, Lanser JB, Roos RA, Bleeker-Wagemakers EM, Frants RR, Ferrari MD.
Terwindt GM, et al. Among authors: storimans cw.
Brain. 1998 Feb;121 ( Pt 2):303-16. doi: 10.1093/brain/121.2.303.
Brain. 1998.
PMID: 9549508
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Familial vascular retinopathy. A preliminary report.
Storimans CW, Oosterhuis JA, van Schooneveld MJ, Bos PJ, Maaswinkel-Mooy PD.
Storimans CW, et al.
Doc Ophthalmol. 1990 Oct;75(3-4):259-61. doi: 10.1007/BF00164839.
Doc Ophthalmol. 1990.
PMID: 2090400
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Serotoninergic status in patients with hereditary vascular retinopathy syndrome.
Storimans CW, Fekkes D, van Dalen A, Bleeker-Wagemakers ED, Oosterhuis JA.
Storimans CW, et al.
Br J Ophthalmol. 1998 Aug;82(8):897-900. doi: 10.1136/bjo.82.8.897.
Br J Ophthalmol. 1998.
PMID: 9828773
Free PMC article.
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[With an eye on... the champagne cork].
Keunen JE, Storimans CW.
Keunen JE, et al. Among authors: storimans cw.
Ned Tijdschr Geneeskd. 1994 Dec 24;138(52):2594-6.
Ned Tijdschr Geneeskd. 1994.
PMID: 7808531
Dutch.
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