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Novel mutations of PKD genes in the Czech population with autosomal dominant polycystic kidney disease

BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disorder caused by mutation in either one of two genes, PKD1 and PKD2. High structural and sequence complexity of PKD genes makes the mutational diagnostics of ADPKD challenging. The present study is...

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Библиографические подробности
Главные авторы: Obeidova, Lena, Elisakova, Veronika, Stekrova, Jitka, Reiterova, Jana, Merta, Miroslav, Tesar, Vladimir, Losan, Frantisek, Kohoutova, Milada
Формат: Artigo
Язык:Inglês
Опубликовано: BioMed Central 2014
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC3992149/
https://ncbi.nlm.nih.gov/pubmed/24694054
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-15-41
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