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Deletion pattern in the dystrophin gene in Duchenne muscular dystrophy patients in northeast India
Duchenne muscular dystrophy (DMD) is an X-linked recessive disorder that affects 1 in 3,500 males and is caused by mutations in the dystrophin gene. In this paper, we have reported DNA analysis of DMD patients by multiplex polymerase chain reaction (PCR) from various states of northeast India. Of th...
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| 主要な著者: | , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Medknow Publications & Media Pvt Ltd
2013
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3724316/ https://ncbi.nlm.nih.gov/pubmed/23914114 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-3147.112777 |
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