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Archives of Ophthalmology

Volumn 130, Issue 2, 2012, Pages 255-257

Novel clinical manifestation of congenital x-linked retinoschisis

(3) Eadie, James A a Luo, Caesar K b Trese, Michael T b

a WILLIAM BEAUMONT HOSPITAL (United States)

b ASSOCIATED RETINAL CONSULTANTS (United States)

Author keywords

[No Author keywords available]

Indexed keywords

RETINOSCHISIN;

ARTICLE; CASE REPORT; CHILD; CONGENITAL X LINKED RETINOSCHISIS; ELECTRORETINOGRAPHY; EXON; FOLLOW UP; GENE MUTATION; HUMAN; MALE; MISSENSE MUTATION; OPTICAL COHERENCE TOMOGRAPHY; PRIORITY JOURNAL; RETINA MACULA DEGENERATION; RETINITIS PIGMENTOSA; RETINOSCHISIS; SCHOOL CHILD; VISUAL ACUITY; VITREOUS HEMORRHAGE;

CHILD; ELECTRORETINOGRAPHY; EYE PROTEINS; HUMANS; MALE; MUTATION, MISSENSE; RETINOSCHISIS; TOMOGRAPHY, OPTICAL COHERENCE; VISION DISORDERS; VISUAL ACUITY; VISUAL FIELDS; VITREOUS HEMORRHAGE;

EID: 84856871792 PISSN: 00039950 EISSN: 15383601 Source Type: Journal
DOI: 10.1001/archopthalmol.2011.1352 Document Type: Article

Times cited : (5)

References (6)

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- Congenital X-linked retinoschisis classification system
- DOI 10.1097/01.iae.0000244290.09499.c1, PII 0000698220060900100014
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2
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3
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- Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes
- Sieving PA, Bingham EL, Roth MS, et al. Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes. Am J Hum Genet. 1990;47 (4):616-621.
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- Sieving, P.A.¹ Bingham, E.L.² Roth, M.S.³

4
- 0030771360
- Positional cloning of the gene associated with X-linked juvenile retinoschisis
- DOI 10.1038/ng1097-164
- Sauer CG, Gehrig A, Warneke-Wittstock R, et al. Positional cloning of the gene associated with X-linked juvenile retinoschisis. Nat Genet. 1997;17(2): 164-170. (Pubitemid 27425948)
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- Sauer, C.G.¹ Gehrig, A.² Warneke-Wittstock, R.³ Marquardt, A.⁴ Ewing, C.C.⁵ Gibson, A.⁶ Lorenz, B.⁷ Jurklies, B.⁸ Weber, B.H.F.⁹

5
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- X-linked retinoschisis in a female with a heterozygous RS1 missense mutation
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