Sensorimotor neuronopathy in ataxia with oculomotor apraxia type 2-Reference-Cited by-同舟云学术

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Sensorimotor neuronopathy in ataxia with oculomotor apraxia type 2

Published:2009-07-17 Issue:3 Volume:40 Page:481-485
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Gazulla José,Benavente Isabel,López-Fraile Isabel Pérez,Modrego Pedro,Koenig Michel

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.21328/fullpdf

Reference31 articles.

1. Identification and characterisation of a large Senataxin (SETX) gene duplication in ataxia with ocular apraxia type 2 (AOA2);Arning;Neurogenetics,2008

2. New familial cerebellar ataxia with hypergonadotropic hypogonadism and sensorineural deafness;Amor;Am J Hum Genet,2001

3. Clinical and molecular findings of ataxia with oculomotor apraxia type 2 in four families;Anheim;Arch Neurol,2008

4. Autosomal recessive ataxia with peripheral neuropathy and elevated AFP: novel mutations in SETX;Asaka;Neurology,2006

5. In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndrome;Bassuk;Neurogenetics,2007

Cited by 16 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. Understanding oocyte ageing;Minerva Obstetrics and Gynecology;2024-06

2. Ataxia and Hypogonadism: a Review of the Associated Genes and Syndromes;The Cerebellum;2023-03-30

3. 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

4. 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

5. Senataxin: A New Guardian of the Female Germline Important for Delaying Ovarian Aging;Frontiers in Genetics;2021-04-29

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