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Sensitivity and Frequencies of Dystrophin Gene Mutations in Thai DMD/BMD Patients As Detected by Multiplex PCR

Background: Duchenne muscular dystrophy (DMD), a lethal X-linked disease affecting 1 in 3500 male births, and its more benign variant, Becker muscular dystrophy (BMD), are caused by mutations in the dystrophin gene. Because of its large size, analysing the whole gene is impractical. Methods have bee...

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Detalhes bibliográficos
Main Authors: Sura, Thanyachai, Eu-ahsunthornwattana, Jakris, Pingsuthiwong, Sarinee, Busabaratana, Manisa
Formato: Artigo
Idioma:Inglês
Publicado em: IOS Press 2008
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3827792/
https://ncbi.nlm.nih.gov/pubmed/18957722
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2008/521568
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