Duchenne and Becker Muscular Dystrophy
- Author(s)
- Hossein Najmabadi, Kimia Kahrizi, Mohammad Khalil Javan, Mandana Hassanzad
- Year
- 2004
- Language
- Persian
- BISAC Code
- MED056000 — Medical / Genetics MED022090 — Medical / Neurology / Muscular Dystrophy
- Scopus Subject Area
- Genetics, Molecular Biology, Neurology, Clinical Medicine, Rehabilitation Sciences
- Target Audience
- Geneticists, neurologists, neuromuscular specialists, rehabilitation clinicians, medical students
- Citation Info
- summary
- This book presents a scientific and research based overview of Duchenne and Becker muscular dystrophies—two of the most common hereditary neuromuscular disorders. It explains the progressive nature of these diseases, their genetic basis, and the molecular mechanisms underlying dystrophin deficiency. The introduction highlights the historical development of muscular dystrophy research, from early clinical descriptions to modern molecular diagnostics. The book focuses on genetic analysis, mutation types, diagnostic methods, carrier detection, and prenatal testing, offering concise yet comprehensive information for students, clinicians, and researchers working in human molecular genetics and neuromuscular medicine.
انتخاب حالت کور رنگی
سرخ کوری سبز کوری آبی کوری سرخ دشوار بینی سبز دشوار بینی آبی دشوار بینی تک رنگ بینی تک رنگ بینی مخروطیتغییر اندازه فونت:
تغییر فاصله بین کلمات:
تغییر فاصله بین خطوط:
تغییر نوع موس:
تغییر نوع موس:
تغییر رنگ ها:
رنگ اصلی:
رنگ دوم:
رنگ سوم: