Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region-Reference-Cited by-同舟云学术

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Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region

Published:2003-06-01 Issue:6 Volume:250 Page:668-671
ISSN:0340-5354
Container-title:Journal of Neurology
language:
Short-container-title:Journal of Neurology

Author:

Hellenbroich Y.,Bubel S.,Pawlack H.,Opitz S.,Vieregge P.,Schwinger E.,Z�hlke C.

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-003-1052-x.pdf

Cited by 52 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. Repeat length in spinocerebellar ataxia type 4 (SCA4) predicts age at onset and disease severity;Journal of Neurology;2024-08-02

2. Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs;Journal of Internal Medicine;2024-07-07

3. SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies;Movement Disorders;2024-03

4. Adaptive Long‐Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4;Movement Disorders;2024-01-10

5. Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine disease;The American Journal of Human Genetics;2024-01

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