Intrafamilial correlation in Friedreich's ataxia
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1981.tb01052.x/fullpdf
Reference24 articles.
1. A determination of the consanguinity rate in the general hospital population of England and Wales;Bell;Ann. Eugen. (Lond.),1940
2. On hereditary ataxia and spastic paraplegia;Bell;Treasury of Human Inheritance,1939
3. A cluster of Friedreich's ataxia in Rimouski, Quebec;Bouchard;Canad. J. Neurol. Sci.,1979
4. A note on the frequency of consanguineous marriages in Reading, England, in 1972/1973;Coleman;Hum. Hered.,1980
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1. A systematic review of disease prevalence, health-related quality of life, and economic outcomes associated with Friedreich’s Ataxia;Current Medical Research and Opinion;2022-08-23
2. Interruptions of the FXN GAA Repeat Tract Delay the Age at Onset of Friedreich’s Ataxia in a Location Dependent Manner;International Journal of Molecular Sciences;2021-07-13
3. Long-term voluntary running prevents the onset of symptomatic Friedreich’s ataxia in mice;Scientific Reports;2020-04-08
4. Mitochondrial damage and senescence phenotype of cells derived from a novel frataxin G127V point mutation mouse model of Friedreich's ataxia;Disease Models & Mechanisms;2020-01-01
5. Prevalence gradients of Friedreich's Ataxia and R1b haplotype in Europe co-localize, suggesting a common Palaeolithic origin in the Franco-Cantabrian ice age refuge;Journal of Neurochemistry;2013-07-17
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