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Muscular Dystrophy Services In United Kingdom
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Manufactured by:Creative Biolabs based inShirley, NEW YORK (USA)
DMD is a progressive muscle wasting disease that affects approximately 1 in 3500 male births. It is caused by mutations in a large 79-exon gene encoding the dystrophin protein. The majority of mutations identified in DMD are frameshift mutations that result in complete loss of dystrophin. Patients typically present at 2-5 years of age with a waddling gait, calf hypertrophy, and difficulties in ...
Manufactured by:Creative Biolabs based inShirley, NEW YORK (USA)
Optimal autophagy activity plays an important protective role in several human diseases, such as neurodegenerative diseases, Parkinson's disease, hereditary myopathy, and melanin-deficient congenital muscular dystrophy. Therefore, monitoring autophagy can provide valuable insights into understanding human pathological mechanisms, developing new drugs, and ...
