GENETICS
HUMAN NUCLEOTIDE EXPANSION DISORDERS
MECHANISMS OF DNA REPEAT EXPANSION MOLECULAR CORRELATES OF FRAGILE X SYNDROME AND FXTAS THE NEGLECTED FRAGILE XMUTATIONS: 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 POLYGLUTAMINE DISEASES THE ENIGMA OF SPINOCEREBELLAR ATAXIA TYPE 6 SPINOCEREBELLAR ATAXIA TYPE 12 AND HUNTINGTON’S DISEASE-LIKE 2: CLUES TO PATHOGENESIS CURRENT ISSUES AND THERAPEUTIC PROSPECTS