Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype-Reference-Cited by-同舟云学术

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Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype

Published:1998-01 Issue:4 Volume:19 Page:187-196
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Ponjavic Vesna,Andréasson Sten,Abrahamson Magnus,Ehinger Berndt,Gieser Linn,Fujita Ricardo,Swaroop Anand

Publisher

Swets & Zeitlinger Publishers

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.1076/opge.19.4.187.2305

Reference22 articles.

1. X-linked retinitis pigmentosa.

2. Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

3. X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosome

4. Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa families

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Retinitis pigmentosa caused by mutations in the ciliaryMAKgene is relatively mild and is not associated with apparent extra-ocular features;Acta Ophthalmologica;2014-11-11

2. Developments in molecular genetics and electrophysiology in inherited retinal disorders;Acta Ophthalmologica Scandinavica;2006-03-30

3. Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes;Ophthalmic Genetics;2003-01

4. Genotype-phenotype correlation in X-linked retinitis pigmentosa 2 (RP2);Ophthalmic Genetics;1999-01

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