Evaluation of multiplex ligation-dependent probe amplification analysis versus multiplex polymerase chain reaction assays in the detection of dystrophin gene rearrangements in an Iranian population subset

BACKGROUND: The Duchenne muscular dystrophy (DMD) gene is located in the short arm of the X chromosome (Xp21). It spans 2.4 Mb of the human genomic DNA and is composed of 79 exons. Mutations in the Dystrophin gene result in DMD and Becker muscular dystrophy. In this study, the efficiency of multiple...

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Hlavní autoři: Nouri, Nayereh, Fazel-Najafabadi, Esmat, Salehi, Mansoor, Hosseinzadeh, Majid, Behnam, Mahdieh, Ghazavi, Mohammad Reza, Sedghi, Maryam
Médium: Artigo
Jazyk:Inglês
Vydáno: Medknow Publications & Media Pvt Ltd 2014
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3950794/
https://ncbi.nlm.nih.gov/pubmed/24627880
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2277-9175.125862
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