Germ cell arrest associated with aSETX mutation in ataxia oculomotor apraxia type 2
Author:
Funder
National Health and Medical Research
Publisher
Elsevier BV
Subject
Developmental Biology,Reproductive Medicine,Obstetrics and Gynecology
Reference11 articles.
1. Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical management;Anheim;Neurogenetics,2010
2. Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients;Anheim;Brain,2009
3. Senataxin plays an essential role with DNA damage response proteins in meiotic recombination and gene silencing;Becherel;PLoS Genet,2013
4. Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study;Criscuolo;Neurology,2006
5. Sensorimotor neuronopathy in ataxia with oculomotor apraxia type 2;Gazulla;Muscle Nerve,2009
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1. RNase H1 facilitates recombinase recruitment by degrading DNA–RNA hybrids during meiosis;Nucleic Acids Research;2023-06-28
2. A novel mouse allele of the DNA/RNA helicase senataxin (Setxspcar3) causing meiotic arrest of spermatocytes and male infertility;2023-04-13
3. Ataxia and Hypogonadism: a Review of the Associated Genes and Syndromes;The Cerebellum;2023-03-30
4. 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
5. R-Loop Formation in Meiosis: Roles in Meiotic Transcription-Associated DNA Damage;Epigenomes;2022-08-24
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