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7. The Friedreich ataxia GAA repeat expansion mutation induces comparable epigenetic changes in human and transgenic mouse brain and heart tissues. Al-Mahdawi S; Pinto RM; Ismail O; Varshney D; Lymperi S; Sandi C; Trabzuni D; Pook M Hum Mol Genet; 2008 Mar; 17(5):735-46. PubMed ID: 18045775 [TBL] [Abstract][Full Text] [Related]
8. Detection of interruptions in the GAA trinucleotide repeat expansion in the FXN gene of Friedreich ataxia. Holloway TP; Rowley SM; Delatycki MB; Sarsero JP Biotechniques; 2011 Mar; 50(3):182-6. PubMed ID: 21486239 [TBL] [Abstract][Full Text] [Related]
9. [Genetic tests: how far should we go? A case of late-onset Friedreich's disease]. Ruolt I; Tranchant C; Warter JM Rev Neurol (Paris); 2000 Dec; 156(12):1148-50. PubMed ID: 11139731 [TBL] [Abstract][Full Text] [Related]
10. Early onset of Friedreich's ataxia in a compound heterozygote. McGovern MC; Stewart M; Morrison PJ; Webb D; Hawkins S Arch Dis Child; 2000 Jul; 83(1):74-5. PubMed ID: 10869006 [TBL] [Abstract][Full Text] [Related]
11. Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with Friedreich's ataxia. Houshmand M; Panahi MS; Nafisi S; Soltanzadeh A; Alkandari FM Mitochondrion; 2006 Apr; 6(2):82-8. PubMed ID: 16581313 [TBL] [Abstract][Full Text] [Related]
12. Heteroduplexes may confuse the interpretation of PCR-based molecular tests for the Friedreich ataxia GAA triplet repeat. Poirier J; Ohshima K; Pandolfo M Hum Mutat; 1999; 13(4):328-30. PubMed ID: 10220147 [No Abstract] [Full Text] [Related]
14. Structural studies on DNA triple helix formed by intronic GAA triplet repeat expansion in Friedreich's ataxia. Jain A; Ahmad F; Rajeswari MR Nucleosides Nucleotides Nucleic Acids; 2003; 22(5-8):1517-9. PubMed ID: 14565456 [No Abstract] [Full Text] [Related]
15. Clinical and genetic correlate in childhood onset Friedreich ataxia. Alikaşifoglu M; Topaloglu H; Tunçbilek E; Ceviz N; Anar B; Demir E; Ozme S Neuropediatrics; 1999 Apr; 30(2):72-6. PubMed ID: 10401688 [TBL] [Abstract][Full Text] [Related]
16. Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion. Labuda M; Labuda D; Miranda C; Poirier J; Soong BW; Barucha NE; Pandolfo M Neurology; 2000 Jun; 54(12):2322-4. PubMed ID: 10881262 [TBL] [Abstract][Full Text] [Related]
17. A novel GAA-repeat-expansion-based mouse model of Friedreich's ataxia. Anjomani Virmouni S; Ezzatizadeh V; Sandi C; Sandi M; Al-Mahdawi S; Chutake Y; Pook MA Dis Model Mech; 2015 Mar; 8(3):225-35. PubMed ID: 25681319 [TBL] [Abstract][Full Text] [Related]
18. GAA repeat polymorphism in Turkish Friedreich's ataxia patients. Yilmaz MB; Koç AF; Kasap H; Güzel AI; Sarica Y; Süleymanova D Int J Neurosci; 2006 May; 116(5):565-74. PubMed ID: 16644517 [TBL] [Abstract][Full Text] [Related]
19. Protocol proposal for Friedreich ataxia molecular diagnosis using fluorescent and triplet repeat primed polymerase chain reaction. Xunclà M; Rodríguez-Revenga L; Madrigal I; Jiménez D; Milà M; Badenas C Transl Res; 2010 Nov; 156(5):309-14. PubMed ID: 20970754 [TBL] [Abstract][Full Text] [Related]
20. Complete FXN deletion in a patient with Friedreich's ataxia. van den Ouweland AM; van Minkelen R; Bolman GM; Wouters CH; Becht-Noordermeer C; Deelen WH; Deelen-Manders JM; Ippel EP; Saris J; Halley DJ Genet Test Mol Biomarkers; 2012 Sep; 16(9):1015-8. PubMed ID: 22691228 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]