CAG repeat expansion in autosomal dominant familial spastic paraparesis: novel expansion in a subset of patients

By Benson K.F.  

Human Molecular Genetics, Vol. 7, Iss. 11, 1998-11 ,pp. : 1779-1786

Oxford University Press

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Cag Repeat Expansion in Autosomal Dominant Pure Spastic Paraplegia Linked to Chromosome 2p21–p24

By Nielsen Jørgen E.   Koefoed Pernille   Abell Kathrine   Hasholt Lis   Eiberg Hans   Fenger Kirsten   Niebuhr Erik   Sørensen Sven Asger  

Human Molecular Genetics, Vol. 6, Iss. 11, 1997-10 ,pp. : 1811-1816

Oxford University Press

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Pms2 is a genetic enhancer of trinucleotide CAG·CTG repeat somatic mosaicism: implications for the mechanism of triplet repeat expansion

By Gomes-Pereira Mário   Fortune M. Teresa   Ingram Laura   McAbney John P.   Monckton Darren G.  

Human Molecular Genetics, Vol. 13, Iss. 16, 2004-08 ,pp. : 1815-1825

Oxford University Press

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SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein

By Nakamura K.  

Human Molecular Genetics, Vol. 10, Iss. 14, 2001-07 ,pp. : 1441-1448

Oxford University Press

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Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy ( SCA7 )

By David G.  

Human Molecular Genetics, Vol. 7, Iss. 2, 1998-02 ,pp. : 165-170

Oxford University Press

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