SETX gene novel mutations in a non-French Canadian with ataxia-oculomotor apraxia type 2
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
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Cited by 5 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. Ataxia with oculomotor apraxia type 2 caused by a novel homozygous mutation in SETX gene, and literature review;Frontiers in Molecular Neuroscience;2022-11-10
2. Heterozygous deletion in exon 6 of STEX gene causing ataxia with oculomotor apraxia type 2 (AOA-2) with ovarian failure;BMJ Case Reports;2021-06
3. Some pathogenic SETX variants are partially conserved during evolution;Gene;2021-03
4. A novel SETX gene mutation producing ataxia with oculomotor apraxia type 2;Acta Neurologica Belgica;2016-01-25
5. A Case of an African American Man With Ataxia and Oculomotor Apraxia 2;Journal of Clinical Neuromuscular Disease;2014-09
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