Non-deletion mutations in Egyptian patients with Duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD) is the most common form of muscular dystrophies affecting approximately 1:3500 male live births. Deletion of the dystrophin gene accounts for approximately 65% of mutations, duplications occur in 6–10% while the remaining 20–30% are point mutations, small deletion/i...
Main Authors: | Rabah M. Shawky, Solaf M. Elsayed, Theodor Todorov, Andree Zibert, Salem Alawbathani, Hartmut H.-J. Schmidt |
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Format: | Article |
Language: | English |
Published: |
SpringerOpen
2014-07-01
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Series: | Egyptian Journal of Medical Human Genetics |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S1110863014000536 |
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