Duchenne muscular dystrophy: A immunohistochemical profile and deletion pattern in dystrophin gene in North Indian population
Background: Duchenne muscular dystrophy (DMD), one of the most common X linked muscular disorder, affecting 1 in 3500 male births and is caused by mutation in dystrophin gene. 65% of DMD cases are caused by large deletion of dystrophin gene, followed by duplication (5-10%) or point mutation (25-30%...
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| Materialtyp: | Artigo |
| Språk: | Inglês |
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Manipal College of Medical Sciences, Pokhara
2017-11-01
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| Serie: | Asian Journal of Medical Sciences |
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| Länkar: | https://www.nepjol.info/index.php/AJMS/article/view/18281 |
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