Spinocerebellar ataxia type 7 presenting as Stargardt's disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Link
http://link.springer.com/content/pdf/10.1007/s00415-007-0740-3.pdf
Reference11 articles.
1. Michalik A, Martin JJ, Van Broeckhoven C (2004) Spinocerebellar ataxia type 7 associated with pigmentary retinal dystrophy. Eur J Hum Genet 12:2–15
2. Stefkova J, Poledne R, Hubacek JA (2004) ATP-binding cassette (ABC) transporters in human metabolism and diseases. Physiol Res 53:235–243
3. Stevanin G, Giunti P, Belal GD, Durr A, Ruberg M, Wood N, Brice A (1998) De novo expansion of intermediate alleles in spinocerebellar ataxia 7. Hum Mol Genet 7:1809–1813
4. Johansson J, Forsgren L, Sandgren O, Brice A, Holmgren G, Holmberg M (1998) Expanded CAG repeats in Swedish spinocerebellar ataxia type 7 (SCA7) patients: effect of CAG repeat length on the clinical manifestation. Hum Mol Genet 7:171–176
5. Aleman TS, Cideciyan AV, Volpe NJ, Stevanin G, Brice A, Jacobson SG (2002) Spinocerebellar ataxia type 7 (SCA7) shows a cone-rod dystrophy phenotype. Exp Eye Res 74:737–745
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1. Macular Dysfunction and Morphology in Spinocerebellar Ataxia Type 7 (SCA 7);Ophthalmic Genetics;2009-01
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