X-Linked Recessive Mutations in Simplex Males With Retinitis Pigmentosa

被引：0

作者：

Brumm, M. V. ^{[1
]}

Branham, K. ^{[1
]}

Othman, M. ^{[1
]}

Karoukis, A. J. ^{[1
]}

Weleber, R. G. ^{[2
]}

Iannaccone, A. ^{[3
]}

Jacobson, S. G. ^{[4
]}

Swaroop, A. ^{[1
,5
]}

Heckenlively, J. R. ^{[1
]}

机构：

[1] Univ Michigan, Kellogg Eye Ctr, Dept Ophthalmol & Visual Sci, Ann Arbor, MI 48109 USA

[2] Oregon Hlth & Sci Univ, Casey Eye Inst, Portland, OR 97201 USA

[3] Univ Tennessee, Dept Ophthalmol, Hlth Sci Ctr, Hamilton Eye Inst, Memphis, TN USA

[4] Univ Penn, Scheie Eye Inst, Dept Ophthalmol, Philadelphia, PA 19104 USA

[5] NEI, Neurobiol Neurodegenerat & Repair Lab, Bethesda, MD 20892 USA

来源：

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2010年 / 51卷 / 13期

关键词：

retinal degenerations: hereditary; gene screening;

D O I：

暂无

中图分类号：

R77 [眼科学];

学科分类号：

100212 ;

摘要：

1399

引用

页数：3

共 50 条

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[7] Fundus autofluorescence in carriers of X-linked recessive retinitis pigmentosa.
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[J]. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2001, 42 (04) : S74 - S74
[8] MAPPING OF THE X-LINKED RECESSIVE RETINITIS-PIGMENTOSA GENE - A REVIEW
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[J]. OPHTHALMIC PAEDIATRICS AND GENETICS, 1990, 11 (02): : 77 - 88
[9] NON-ALLELIC MUTATIONS IN X-LINKED RETINITIS PIGMENTOSA
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[J]. CLINICAL GENETICS, 1989, 35 (05) : 338 - 342
[10] HETEROGENEITY IN X-LINKED RETINITIS PIGMENTOSA
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EVANS, HJ
[J]. CYTOGENETICS AND CELL GENETICS, 1989, 51 (1-4): : 1110 - 1110

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