Genetic analysis of early onset cerebellar ataxia with retained tendon reflexes in four Tunisian families
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2001.590407.x/fullpdf
Reference23 articles.
1. clinical and genetic heterogeneity in early onset cerebellar ataxia with retained tendon reflexes;Filla;J Neurol Neurosurg Psychiatry,1990
2. Localization of Friedreich ataxia phenotype associated with selective vitamin E deficiency to proximal 8q by homozygosity mapping;Benhamida;Nat Genet,1993
3. Mapping of Friedreich's ataxia locus by identification of recombination events in patients homozygous by descent;Monros;Eur J Hum Genet,1994
4. late onset Friedreich's ataxia: clinical features and mapping of mutation to the FRDA locus;DeMichele;J Neurol Neurosurg Psychiatry,1994
5. Cerebellar ataxia with retained tendon reflexes: a clinical and genetic study of a disorder distinct from Friedreich's ataxia;Harding;J Neurol Neurosurg Psychiatry,1981
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1. Other autosomal recessive and childhood ataxias;Handbook of Clinical Neurology;2012
2. Epidemiology and population genetics of degenerative ataxias;Handbook of Clinical Neurology;2012
3. Genetic diseases in the Tunisian population;American Journal of Medical Genetics Part A;2010-12-28
4. Friedreich’s ataxia: clinical heterogeneity in two sisters;Neurological Sciences;2006-06
5. Genetic ataxia;Neurologic Clinics;2002-08
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