Transcriptional Complexity in Autosomal Recessive Polycystic Kidney Disease

BACKGROUND AND OBJECTIVES: Autosomal recessive polycystic kidney disease (ARPKD) is caused by mutations in the PKHD1 gene. The longest open reading frame comprises 66 exons encoding polyductin or fibrocystin, a type I transmembrane protein with 4074 amino acids. Functional investigations are conside...

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Detaylı Bibliyografya
Asıl Yazarlar: Frank, Valeska, Zerres, Klaus, Bergmann, Carsten
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society of Nephrology 2014
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Original Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4186505/
https://ncbi.nlm.nih.gov/pubmed/25104275
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.00920114
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