A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeats-Reference-Cited by-同舟云学术

A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeats

Published:2010-02 Issue:2 Volume:37 Page:284-293
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Boy Jana,Schmidt Thorsten,Schumann Ulrike,Grasshoff Ute,Unser Samy,Holzmann Carsten,Schmitt Ina,Karl Tim,Laccone Franco,Wolburg Hartwig,Ibrahim Saleh,Riess Olaf

Publisher

Elsevier BV

Subject

Neurology

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5. Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado–Joseph disease locus;Cancel;Am. J. Hum. Genet.,1995

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