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2. Molecular analysis of Friedreich's ataxia locus in the Indian population. Mukerji M; Choudhry S; Saleem Q; Padma MV; Maheshwari MC; Jain S Acta Neurol Scand; 2000 Oct; 102(4):227-9. PubMed ID: 11071107 [TBL] [Abstract][Full Text] [Related]
3. Friedreich's ataxia. Revision of the phenotype according to molecular genetics. Schöls L; Amoiridis G; Przuntek H; Frank G; Epplen JT; Epplen C Brain; 1997 Dec; 120 ( Pt 12)():2131-40. PubMed ID: 9448568 [TBL] [Abstract][Full Text] [Related]
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6. Challenges ahead for trials in Friedreich's ataxia. Lynch DR; Kichula E Lancet Neurol; 2016 Dec; 15(13):1300-1301. PubMed ID: 27839636 [No Abstract] [Full Text] [Related]
7. Intronic GAA triplet repeat expansion in Friedreich's ataxia presenting with pure sensory ataxia. Berciano J; Combarros O; De Castro M; Palau F J Neurol; 1997 Jun; 244(6):390-1. PubMed ID: 9249627 [No Abstract] [Full Text] [Related]
8. Genetic abnormalities in Friedreich's ataxia. Filla A; De Michele G; Cocozza S N Engl J Med; 1997 Apr; 336(14):1021-2; author reply 1022. PubMed ID: 9091786 [No Abstract] [Full Text] [Related]
9. Genetic abnormalities in Friedreich's ataxia. Dutka DP; Nunez DJ N Engl J Med; 1997 Apr; 336(14):1021; author reply 1022. PubMed ID: 9091785 [No Abstract] [Full Text] [Related]
10. Genetic abnormalities in Friedreich's ataxia. Madhani HD N Engl J Med; 1997 Apr; 336(14):1022; author reply 1022-3. PubMed ID: 9091787 [No Abstract] [Full Text] [Related]
11. The GAA repeat expansion in intron 1 of the frataxin gene is related to the severity of cardiac manifestation in patients with Friedreich's ataxia. Bit-Avragim N; Perrot A; Schöls L; Hardt C; Kreuz FR; Zühlke C; Bubel S; Laccone F; Vogel HP; Dietz R; Osterziel KJ J Mol Med (Berl); 2001; 78(11):626-32. PubMed ID: 11269509 [TBL] [Abstract][Full Text] [Related]
12. Friedreich's ataxia: clinical aspects and pathogenesis. Pandolfo M Semin Neurol; 1999; 19(3):311-21. PubMed ID: 12194387 [TBL] [Abstract][Full Text] [Related]
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