Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene region-Reference-Cited by-同舟云学术

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Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene region

Published:1995-05-01 Issue:5 Volume:4 Page:931-935
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Bergen A. A. B.,Brink J. B. t.,Riemslag F.,Schuurman E. J. M.,Tijmes N.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/4/5/931/2089374/4-5-931.pdf

Cited by 9 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. Mutations in theCACNA1F andNYX genes in British CSNBX families;Human Mutation;2003-01-27

2. The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein;Nature Genetics;2000-11

3. Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness;Nature Genetics;2000-11

4. Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian family;European Journal of Human Genetics;1999-06-22

5. An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness;Nature Genetics;1998-07

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