Human Nucleotide Expansion Disorders /
| Autor Corporativo: | |
|---|---|
| Otros Autores: | , |
| Formato: | eBook |
| Lenguaje: | English |
| Publicado: |
Berlin, Heidelberg :
Springer Berlin Heidelberg : Imprint: Springer,
2006.
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| Edición: | 1st ed. 2006. |
| Colección: | Nucleic Acids and Molecular Biology,
19 |
| Materias: |
Tabla de Contenidos:
- 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.