Učitavanje...
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...
Spremljeno u:
| Glavni autori: | , , |
|---|---|
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
American Society of Nephrology
2014
|
| Teme: | |
| Online pristup: | 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 |
| Oznake: |
Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!
|