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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Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion

By van Regenmorter N.  

Human Molecular Genetics, Vol. 7, Iss. 2, 1998-02 ,pp. : 177-186

Oxford University Press

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A novel trinucleotide repeat expansion at chromosome 3q26.2 identified by a CAG/CTG repeat expansion detection array

By Holmes S.   Wentzell J.   Seixas A.   Callahan C.   Silveira I.   Ross C.   Margolis R.  

Human Genetics, Vol. 120, Iss. 2, 2006-09 ,pp. : 193-200

Springer Publishing Company

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Dnmt1 deficiency promotes CAG repeat expansion in the mouse germline

By Dion Vincent   Lin Yunfu   Hubert Leroy   Waterland Robert A.   Wilson John H.  

Human Molecular Genetics, Vol. 17, Iss. 9, 2008-05 ,pp. : 1306-1317

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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