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Identification of mutations in the repeated part of the autosomal dominant polycystic kidney disease type 1 gene, PKD1, by long-range PCR.

We have used long-range PCR to identify mutations in the duplicated part of the PKD1 gene. By means of a PKD1-specific primer in intron 1, an approximately 13.6-kb PCR product that includes exons 2-15 of the PKD1 gene has been used to search for mutations, by direct sequence analysis. This region co...

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Detalhes bibliográficos
Main Authors: Thomas, R, McConnell, R, Whittacker, J, Kirkpatrick, P, Bradley, J, Sandford, R
Formato: Artigo
Idioma:Inglês
Publicado em: 1999
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1378073/
https://ncbi.nlm.nih.gov/pubmed/10364515
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