AFX1 and p54 nrb : fine mapping, genomic structure, and exclusion as candidate genes of X-linked dystonia parkinsonism-Reference-Cited by-同舟云学术

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AFX1 and p54 nrb : fine mapping, genomic structure, and exclusion as candidate genes of X-linked dystonia parkinsonism

Published:1997-09-15 Issue:5-6 Volume:100 Page:569-572
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

Peters Usha,Haberhausen Gerd,Kostrzewa Markus,Nolte Dagmar,Müller U.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s004390050553.pdf

Cited by 18 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. Further delineation of the phenotypic spectrum associated with hemizygous loss‐of‐function variants in NONO;American Journal of Medical Genetics Part A;2019-12-28

2. Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants inNONO;Journal of Medical Genetics;2016-08-22

3. New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3);European Journal of Human Genetics;2015-01-21

4. Paraspeckle protein p54nrb links Sox9-mediated transcription with RNA processing during chondrogenesis in mice;Journal of Clinical Investigation;2008-09-02

5. The Hexosamine Signaling Pathway: Deciphering the "O-GlcNAc Code";Science's STKE;2005-11-29

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