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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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Detalhes bibliográficos
Main Authors: Nouri, Nayereh, Fazel-Najafabadi, Esmat, Salehi, Mansoor, Hosseinzadeh, Majid, Behnam, Mahdieh, Ghazavi, Mohammad Reza, Sedghi, Maryam
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications & Media Pvt Ltd 2014
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Acesso em linha: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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