Journal Articles

Evans-Galea MV., Corben LA., Hasell J., Galea CA., Fahey MC., du Sart D., Delatycki MB. A novel deletion-insertion mutation identified in exon 3 of FXN in two siblings with a severe Friedreich ataxia phenotype. Neurogenetics 12 (4) : 307 - 313(2011) PubMed