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Human Nucleotide Expansion Disorders (Nucleic Acids and Molecular Biology, Band 19)
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Human Nucleotide Expansion Disorders (Nucleic Acids and Molecular Biology, Band 19) - Paperback

2010, ISBN: 9783642069970

Springer, Taschenbuch, Auflage: Softcover reprint of hardcover 1st ed. 2006, 312 Seiten, Publiziert: 2010-11-20T00:00:01Z, Produktgruppe: Buch, Hersteller-Nr.: 8 black & white tables, bio… More...

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Human Nucleotide Expansion Disorders Michael Fry Editor
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Human Nucleotide Expansion Disorders Michael Fry Editor - new book

ISBN: 9783642069970

Human neurological and neuromuscular disorders caused by nucleotide expansion are the focus of growing interest of practicing physicians and of interested biomedical researchers. This vol… More...

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Human Nucleotide Expansion Disorders
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Human Nucleotide Expansion Disorders - Paperback

2010

ISBN: 9783642069970

Hardcover

Erscheinungsdatum: 20.11.2010, Medium: Taschenbuch, Einband: Kartoniert / Broschiert, Titel: Human Nucleotide Expansion Disorders, Auflage: Softcover reprint of hardcover 1st ed. 2006, Re… More...

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Human Nucleotide Expansion Disorders - Usdin, Karen (Herausgeber); Fry, Michael (Herausgeber)
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Usdin, Karen (Herausgeber); Fry, Michael (Herausgeber):
Human Nucleotide Expansion Disorders - Paperback

2010, ISBN: 3642069975

Hardcover

Softcover reprint of hardcover 1st ed. 2006 Kartoniert / Broschiert Genetik, Medizin, Biochemie, Zellbiologie (Zytologie), DNA; DNAInstability; Glutamin; Polyglutamine; RNA-mediatedPath… More...

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Human Nucleotide Expansion Disorders - Usdin, Karen (Herausgeber); Fry, Michael (Herausgeber)
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Usdin, Karen (Herausgeber); Fry, Michael (Herausgeber):
Human Nucleotide Expansion Disorders - Paperback

2010, ISBN: 3642069975

Hardcover

Softcover reprint of hardcover 1st ed. 2006 Kartoniert / Broschiert Genetik, Medizin, Biochemie, Zellbiologie (Zytologie), DNA; DNAInstability; Glutamin; Polyglutamine; RNA-mediatedPath… More...

Shipping costs:Versandkostenfrei innerhalb der BRD. (EUR 0.00) MARZIES.de Buch- und Medienhandel, 14621 Schönwalde-Glien
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Bibliographic data of the best matching book

Details of the book
Human Nucleotide Expansion Disorders Michael Fry Editor
Author:
Title:
ISBN:

9783642069970


Human neurological and neuromuscular disorders caused by nucleotide expansion 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 authors discuss molecular, clinical and pathological aspects of the diseases as well as our current understanding of their underlying mechanisms.

Details of the book - Human Nucleotide Expansion Disorders Michael Fry Editor


EAN (ISBN-13): 9783642069970
ISBN (ISBN-10): 3642069975
Hardcover
Paperback
Publishing year: 2010
Publisher: Springer Berlin Heidelberg Core >1 >T
312 Pages
Weight: 0,474 kg
Language: eng/Englisch

Book in our database since 2012-01-11T06:18:58+00:00 (London)
Detail page last modified on 2024-03-03T09:27:29+00:00 (London)
ISBN/EAN: 9783642069970

ISBN - alternate spelling:
3-642-06997-5, 978-3-642-06997-0
Alternate spelling and related search-keywords:
Book author: fry michael
Book title: expansion, molecular biology

Information from Publisher

Author: Michael Fry
Title: Nucleic Acids and Molecular Biology; Human Nucleotide Expansion Disorders
Publisher: Springer; Springer Berlin
294 Pages
Publishing year: 2010-11-20
Berlin; Heidelberg; DE
Printed / Made in
Language: English
219,99 € (DE)

BC; Hardcover, Softcover / Medizin/Nichtklinische Fächer; Neurowissenschaften; Verstehen; DNA; DNA Instability; Glutamin; Nucleotide; Polyglutamine; RNA-mediated Pathology; Repeat Expansion Diseases; Neuroscience; Medical Genetics; Cell Biology; Biochemistry; Genetik, Medizin; Zellbiologie (Zytologie); Biochemie; BB

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.

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