Human Nucleotide Expansion Disorders / edited by Michael Fry, Karen Usdin
Contributor(s): Fry, Michael, editor literario
| Usdin, Karen, editor literario
Material type: 
E-bookSeries: Publisher: Berlin, Heidelberg : Springer International Publishing, 2006Description: 1 recurso en línea (XVII, 293 p.).ISBN: 9783540333364.Subject: NucleótidosOnline resources: Acceso a este recurso digital (usuarios Universidad Europea de Madrid)
Summary: Human neurological and neuromuscular disorders caused by nucleotide expansion, first discovered in 1991, are the focus of growing interest of practicing physicians and of interested biomedical researchers. This volume represents a comprehensive and up-to-date description of many of the better-studied disorders. The expert authors discuss molecular, clinical and pathological aspects of the diseases as well as our current understanding of their underlying mechanisms. Of special interest are ideas and initial results of the different therapeutic strategies that can be employed to overcome some of the disorders. As a summary of the state-of-the-art research in this field, this book is of value to human geneticists, molecular biologists and biochemists as well as to practicing neurologists and pediatricians
| Item type | Current library | Collection | Call number | Copy number | Status | Date due | Barcode | Item holds | |
|---|---|---|---|---|---|---|---|---|---|
LIBRO-E NO PRÉSTAMO
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Madrid Digital Acceso Electrónico (UEM) | Ciencias de la Salud | QP625.N89 M86 2006 EB (Browse shelf(Opens below)) | .i11549117 | Acceso electrónico | eBOOK .i11549117 |
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Human neurological and neuromuscular disorders caused by nucleotide expansion, first discovered in 1991, are the focus of growing interest of practicing physicians and of interested biomedical researchers. This volume represents a comprehensive and up-to-date description of many of the better-studied disorders. The expert authors discuss molecular, clinical and pathological aspects of the diseases as well as our current understanding of their underlying mechanisms. Of special interest are ideas and initial results of the different therapeutic strategies that can be employed to overcome some of the disorders. As a summary of the state-of-the-art research in this field, this book is of value to human geneticists, molecular biologists and biochemists as well as to practicing neurologists and pediatricians
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