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Annual Review of Neuroscience, ISSN 0147-006X, 2007, Volume 30, Issue 1, pp. 575 - 621
The discovery that expansion of unstable repeats can cause a variety of neurological disorders has changed the landscape of disease-oriented research for... 
Unstable repeats | Polyglutamine | Ataxin | Frataxin | Myotonic dystrophy | Huntington disease | Ataxia | Fragile X syndrome | Mental retardation | Spinal bulbar muscular atrophy | SPINOCEREBELLAR ATAXIA TYPE-1 | UBIQUITIN-PROTEASOME SYSTEM | unstable repeats | fragile X syndrome | polyglutamine | NEUROSCIENCES | X MENTAL-RETARDATION | frataxin | myotonic dystrophy | mental retardation | HUNTINGTONS-DISEASE GENE | ataxia | spinal bulbar muscular atrophy | MACHADO-JOSEPH-DISEASE | ataxin | TRANSGENIC MOUSE MODEL | DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY | DOMINANT CEREBELLAR-ATAXIA | BULBAR MUSCULAR-ATROPHY | FMR1 KNOCKOUT MICE | Fragile X Syndrome - genetics | Heredodegenerative Disorders, Nervous System - genetics | Genetic Predisposition to Disease - genetics | Cerebellar Ataxia - metabolism | Brain - physiopathology | Fragile X Syndrome - physiopathology | Humans | Peptides - genetics | Fragile X Syndrome - metabolism | Heredodegenerative Disorders, Nervous System - physiopathology | Mutation - genetics | Huntington Disease - metabolism | Brain - metabolism | Cerebellar Ataxia - physiopathology | Animals | Cerebellar Ataxia - genetics | Peptides - metabolism | Huntington Disease - genetics | Trinucleotide Repeat Expansion - genetics | Heredodegenerative Disorders, Nervous System - metabolism | Huntington Disease - physiopathology | Trinucleotide repeats | Care and treatment | Genetic aspects | Diagnosis
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