Tohru Matsuura

Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10

Takanori Yamagata, Huda Y. Zoghbi, Caleb F. Davis, 2000, Nature Genetics.

Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n.

Yuko Saito, Mari Yoshida, Fumitoshi Ishino, 2009, American journal of human genetics.

Unpaired structures in SCA10 (ATTCT)n.(AGAAT)n repeats.

Tetsuo Ashizawa, Yuri L Lyubchenko, R. Sinden, 2003, Journal of molecular biology.

Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement.

Koji Abe, Akio Koizumi, Hiroko Okuda, 2011, American journal of human genetics.

Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10.

Stefan M Pulst, Tetsuo Ashizawa, S. Pulst, 2002, Archives of neurology.

Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20.

Melanie Bahlo, Elsdon Storey, E. Storey, 2004, Brain : a journal of neurology.

Human branch point consensus sequence is yUnAy

Kinji Ohno, Akio Masuda, A. Masuda, 2008, Nucleic acids research.

In vitro and in silico analysis reveals an efficient algorithm to predict the splicing consequences of mutations at the 5′ splice sites

Kinji Ohno, Gen Sobue, Akio Masuda, 2007, Nucleic acids research.