Genetic Instabilities and Neurological Diseases

This book PDF is perfect for those who love Medical genre, written by Robert D. Wells and published by Elsevier which was released on 13 October 2011 with total hardcover pages 784. You could read this book directly on your devices with pdf, epub and kindle format, check detail and related Genetic Instabilities and Neurological Diseases books below.

Genetic Instabilities and Neurological Diseases
Author : Robert D. Wells
File Size : 55,9 Mb
Publisher : Elsevier
Language : English
Release Date : 13 October 2011
ISBN : 9780080463773
Pages : 784 pages
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Genetic Instabilities and Neurological Diseases by Robert D. Wells Book PDF Summary

Genetic Instabilities and Neurological Diseases covers DNA repeat instability and neurological disorders, covering molecular mechanisms of repeat expansion, pathogenic mechanisms, clinical phenotype, parental gender effects, genotype-phenotype correlation, and diagnostic applications of the molecular data. This updated edition provides updates of these repeat expansion mutations, including the addition of many new chapters, and old chapters rewritten as extensions of the previous edition. This book is an invaluable reference source for neuroscientists, geneticists, neurologists, molecular biologists, genetic counsellors and students. Contributions by most of the principal research teams in the area, edited by world-renowned leaders Lays the background for future investigations on related diseases

Genetic Instabilities and Neurological Diseases

Genetic Instabilities and Neurological Diseases covers DNA repeat instability and neurological disorders, covering molecular mechanisms of repeat expansion, pathogenic mechanisms, clinical phenotype, parental gender effects, genotype-phenotype correlation, and diagnostic applications of the molecular data. This updated edition provides updates of these repeat expansion mutations, including the addition of many new

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Genetic Instabilities and Hereditary Neurological Diseases

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Till recently, mutations in genes were described in textbooks as deletions or point mutations. These mutations can be inherited from a parent or they are de novo alterations. The discovery in 1991 that human disease can be caused by large-scale ex pansion of highly unstable trinucleotide repeats has elucidated a new

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There have been remarkable advances towards discovering agents that exhibit selectivity and sequence-specificity for DNA, as well as understanding the interactions that underlie its propensity to bind molecules. This progress has important applications in many areas of biotechnology and medicine, notably in cancer treatment as well as in future gene

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