Over 30 different forms and subtypes of the inherited neuromuscular illnesses known as muscular dystrophy have been identified, and there are still a number of others that need to be identified and categorized. The many muscular dystrophies, the genes associated with each subtype, disease diagnosis, management, and therapy possibilities are all thoroughly examined in this book. Even though each individual kind and subtype of muscular dystrophy has a unique gene associated with its causation, the majority of these types share clinical symptoms, making molecular identification essential for both patient care and disease diagnosis. This insightful book presents discussions of the already available diagnostic approaches that have changed clinical research combined with comments on the ongoing analyses that show promise for future therapeutic approaches.
৳12598 ৳13598-7.35%
- SKU: 9781632424181
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