Facioscapulohumeral Muscular Dystrophy (FSHD)
Clinical Medicine and Molecular Cell Biology
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Facioscapulohumeral Muscular Dystrophy (FSHD) by David N. Cooper
Book DescriptionFacioscapulohumeral muscular dystrophy (FSHD) is a genetic disorder involving slowly progressive muscle degeneration in which the muscles of the face, shoulder blades and upper arms are among the most severely affected. It is the third most common inherited muscular dystrophy, affecting 1 in 20,000. The search for the molecular basis of the disease is of interest to all genetic researchers, involving a deletion outside a coding region resulting in over-expression of adjacent genes. This volume summarizes the current understanding of the disorder, including clinical, molecular and therapeutic aspects.
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Book DetailsISBN: 9781859962442
(234mm x 156mm x 23mm)
Imprint: Garland Publishing Inc
Publisher: Taylor & Francis Inc
Publish Date: 1-Jan-2004
Country of Publication: United States
Books By Author David N. Cooper
Handbook of Human Molecular Evolution, Hardback (August 2008)
"This splendid compendium... will be the standard reference work for years to come: a handbook to browse, to consult, to look things up in, and to read with pleasure, wonder and post-Darwinian exhilaration.
Encyclopedia of the Human Genome, Hardback (June 2003)
Deals with the scientific basis of human genetics and genomics research and its ethical, philosophical, and commercial ramifications. This encyclopedia presents an overview of research and its applications, and examines many peripheral topics surrounding the field, such as law, ethics, medicine and public health, history, religion and industry.
Functional Analysis of the Human Genome, Hardback (June 1995)» View all books by David N. Cooper
This volume is an overview of the relationship between structure and function in the human genome, and a detailed description of some of the important methodologies for unravelling the function of genes and genomic structures.
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