RPGR Transcription Studies in Mouse and Human Tissues Reveal a Retina-Specific Isoform That Is Disrupted in a Patient With X-Linked Retinitis Pigmentosa-Reference-Cited by-同舟云学术

RPGR Transcription Studies in Mouse and Human Tissues Reveal a Retina-Specific Isoform That Is Disrupted in a Patient With X-Linked Retinitis Pigmentosa

Published:1999-08-01 Issue:8 Volume:8 Page:1571-1578
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Kirschner R.,Rosenberg T.,Schultz-Heienbrok R.,Lenzner S.,Feil S.,Roepman R.,Cremers F. P. M.,Ropers H.-H.,Berger W.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/8/8/1571/1659473/8-8-1571.pdf

Reference28 articles.

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

2. Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests.

3. A Novel Locus (RP24) for X-linked Retinitis Pigmentosa Maps to Xq26-27

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