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Duchenne Muscular Dystrophy(Monographs on Medical Genetics)
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Based on the author's study of some 200 patients and a detailed review of the literature, this volume provides a comprehensive and clinical account of all aspects of Duchenne muscular dystrophy--the second most common genetic disorder affecting humans. During the last decade, biochemists and molecular biologists have made a huge effort to understand the basic molecular defect. In 1986, when this book was first in press, Professor Emery was able to predict with some confidence that the locus of the gene responsible would soon be identified. The publication of this revised paperback edition offers the opportunity to bring his account up-to-date with a discussion of the isolation of the gene and its unexpected size and complexity, followed by the characterization of the related protein dystrophin, a component of skeletal muscle.
Genre: Duchenne muscular dystrophy, Diagnosis
Format: Paperback
Published: 1988
Pages: 317
Publisher: Oxford University Press
ISBN: 9780192617989
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Condition Descriptions
Our conditions mean the following:
- New - a brand new book
- Almost New - appears new but is actually secondhand.
- Very Good - only minor imperfections such as minor scuffs to edge or cover or a price written in pencil or shop sticker.
- Standard Secondhand - Clearly been read before, but not too bad. We do not recommend these for gifting. Spines usually creased. Could also include creases or folds to cover, some writing such as in the cover or elsewhere, underlining or highlighting, but might not do. Possibly some stains or marks. Similar in general to books in any secondhand shop or charity shop.
- Poor Condition - Usually this will have a specific problem such as writing inside, water damage, missing dust jacket, heavy staining, large creases or cuts. These are readable copies but not nice ones. On other websites this condition is called 'Acceptable' or 'Fair' , but we want to be more honest.
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