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High Resolution Melt analysis for mutation screening in PKD1 and PKD2

BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disorder. It is characterized by focal development and progressive enlargement of renal cysts leading to end-stage renal disease. PKD1 and PKD2 have been implicated in ADPKD pathogenesis but genetic...

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Detalles Bibliográficos
Autores principales:	Bataille, Stanislas, Berland, Yvon, Fontes, Michel, Burtey, Stéphane
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2011
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206831/ https://www.ncbi.nlm.nih.gov/pubmed/22008521 http://dx.doi.org/10.1186/1471-2369-12-57

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