New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease

BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disease. The disease is caused by mutations of the PKD1 (affecting roughly 85% of ADPKD patients) and PKD2 (affecting roughly 14% of ADPKD patients) genes, although in several ADPKD families, the PKD...

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Detaylı Bibliyografya
Asıl Yazarlar: Stekrova, Jitka, Reiterova, Jana, Svobodova, Stanislava, Kebrdlova, Vera, Lnenicka, Petr, Merta, Miroslav, Viklicky, Ondrej, Kohoutova, Milada
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2009
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2736583/
https://ncbi.nlm.nih.gov/pubmed/19686598
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-10-78
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