Muscular Dystrophy: Methods and Protocols (Methods in Molecular Medicine)
Katherine Bushby (Ed.)
€ 196.43
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Description for Muscular Dystrophy: Methods and Protocols (Methods in Molecular Medicine)
Hardcover. Assembles a collection of key techniques for the analysis of DNA and protein from patients suspected to suffer from muscular dystrophy. This work explores various DNA techniques that focus on both the X-linked muscular dystrophies and the autosomal recessive muscular dystrophies. It is suitable for diagnostic laboratories, and clinicians. Editor(s): Bushby, Katherine; Anderson, Louise V.B. Series: Methods in Molecular Medicine. Num Pages: 458 pages, biography. BIC Classification: MBG; MMFM; MNS. Category: (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly; (UU) Undergraduate. Dimension: 235 x 155 x 30. Weight in Grams: 866.
The term muscular dystrophy (MD) describes a group of primary genetic disorders of muscle that often have a distinctive and recognizable clinical p- notype, accompanied by characteristic, but frequently not pathognomonic, pathological features. Research into the molecular basis of the MDs by a c- bination of positional cloning and candidate gene analysis has provided the basis for a reclassification of these disorders, with genetic and protein data augmenting traditional clinically based nomenclature. These findings have brought insights into the molecular pathogenesis of MD, with an increasing number of potential pathways involved in arriving at a dystrophic phenotype. Some ... Read more
The term muscular dystrophy (MD) describes a group of primary genetic disorders of muscle that often have a distinctive and recognizable clinical p- notype, accompanied by characteristic, but frequently not pathognomonic, pathological features. Research into the molecular basis of the MDs by a c- bination of positional cloning and candidate gene analysis has provided the basis for a reclassification of these disorders, with genetic and protein data augmenting traditional clinically based nomenclature. These findings have brought insights into the molecular pathogenesis of MD, with an increasing number of potential pathways involved in arriving at a dystrophic phenotype. Some ... Read more
Product Details
Publisher
Humana Press
Format
Hardback
Publication date
2001
Series
Methods in Molecular Medicine
Condition
New
Weight
866g
Number of Pages
458
Place of Publication
Totowa, NJ, United States
ISBN
9780896036956
SKU
V9780896036956
Shipping Time
Usually ships in 15 to 20 working days
Ref
99-15
Reviews for Muscular Dystrophy: Methods and Protocols (Methods in Molecular Medicine)
This book will be of primary interest to pathologists, geneticists, and neurologists actively engaged in molecular testing of the patients with muscular dystrophy. . .This is a highly practical book aimed at scientists actively engaged in doing the molecular tests. Diseases covered include the X-linked muscular dystrophies and the autosomal recessive muscular dystrophies. Both DNA and protein methods are covered. ... Read more