Human Nucleotide Expansion Disorders - Fry, Michael; Usdin, Karen; SpringerLink (Online service) (Berlin, Heidelberg : Springer Berlin Heidelberg : Imprint: Springer, 2006)
Molecular Bases of Nucleotide Expansions -- Mechanisms of DNA Repeat Expansion -- Disorders Associated with Non-coding Repeats -- Molecular Correlates of Fragile X Syndrome and FXTAS -- The Neglected Fragile X Mutations: FRAXE and FRAXF -- Friedreich Ataxia -- Dodecamer Repeat Expansion in Progressive Myoclonus Epilepsy 1 -- Myotonic Dystrophies Types 1 and 2 -- Spinocerebellar Ataxia Type 8 -- Recent Progress in Spinocerebellar Ataxia Type 10 -- Disorders Associated with Coding Repeats -- Polyglutamine Diseases -- The Enigma of Spinocerebellar Ataxia Type 6 -- Disorders Associated with Repeats in an Undetermined Location -- Spinocerebellar Ataxia Type 12 and Huntington's Disease-Like 2: Clues to Pathogenesis -- Postscript -- Current Issues and Therapeutic Prospects.
Keywords: Neurobiology; Neurosciences; Human genetics; Cell biology; Biochemistry; Neurobiology; Neurosciences; Human Genetics; Cell Biology; Biochemistry, general