Title: | Trinucleotide repeat disorders |
Journal : | Annual review of neuroscience, 30 |
Authors: | Orr HT, Author ; Zoghbi HY |
Material Type: | Article |
Publication Date: | 2007 |
Size: | p 575 |
Languages: | English |
Keywords : | AR gene ; autosomal dominant spinocerebellar ataxia type 1 ; autosomal dominant spinocerebellar ataxia type 2 ; autosomal dominant spinocerebellar ataxia type 3 ; CAG triplet repeats ; dentato-rubro-pallido-luysian atrophy ; DMPK gene ; fragile X syndrome ; frataxin ; Friedreich ataxia ; FXN gene ; gène ZNF9 ; genotype-phenotype correlation ; huntingtin ; Huntington disease ; Kennedy disease ; myotonic dystrophy ; myotonic dystrophy type 1 ; myotonic dystrophy type 2 ; phenotypic heterogeneity ; physiopathology ; repeated sequence amplification ; reviews ; spinocerebellar ataxia ; triplet repeats |
Pubmed / DOI : | DOI : 10.1146/annurev.neuro.29.051605.113042 / Pubmed : 17417937 |
Link for e-copy: | http://www.ncbi.nlm.nih.gov/pubmed/17417937 |