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Trinucleotide expansions disease

Keywords Cerebellar ataxias Dentatorubral pallidoluysian atrophy Fragile X syndrome Friedreich ataxia Huntington disease Myotonic dystrophy Spinobulbar muscular atrophy Trinucleotide expansion diseases... [Pg.320]

Among the trinucleotide-expansion diseases, it is still not yet clear what accounts for the sensitivity of nervous tissue to the altered genotype and what accounts for the selective vulnerability of different brain regions among the various diseases. However, some progress is being made. A feature of the Qn-expansion diseases and An-expansion diseases, is the presence of (or propensity to form) aberrant protein deposits in affected brain regions. In this respect, these diseases are similar to the... [Pg.348]

See other pages where Trinucleotide expansions disease is mentioned: [Pg.319]    [Pg.320]    [Pg.321]    [Pg.322]    [Pg.322]    [Pg.323]    [Pg.325]    [Pg.327]    [Pg.328]    [Pg.331]    [Pg.333]    [Pg.335]    [Pg.337]    [Pg.339]    [Pg.341]    [Pg.343]    [Pg.345]    [Pg.347]    [Pg.348]    [Pg.349]    [Pg.351]    [Pg.353]    [Pg.355]    [Pg.357]   
See also in sourсe #XX -- [ Pg.324 ]



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Trinucleotide expansion

Trinucleotides

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