Novel polymorphic AluYb8 insertion in the WNK1 gene is associated with blood pressure variation in Europeans

Mutations in WNK1 and WNK4 cause familial hypertension, the Gordon syndrome. WNK1 and WNK4 conserved noncoding regions were targeted to polymorphism screening using DHPLC and DGGE. The scan identified an undescribed polymorphic AluYb8 insertion in WNK1 intron 10. Screening in primates revealed that...

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Detalhes bibliográficos
Main Authors: Putku, Margus, Kepp, Katrin, Org, Elin, Sõber, Siim, Comas, David, Viigimaa, Margus, Veldre, Gudrun, Juhanson, Peeter, Hallast, Pille, Tõnisson, Neeme, Shaw-Hawkins, Sue, Caulfield, Mark J, Khusnutdinova, Elza, Kožich, Viktor, Munroe, Patricia B, Laan, Maris
Formato: Artigo
Idioma:Inglês
Publicado em: Wiley Subscription Services, Inc., A Wiley Company 2011
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3298642/
https://ncbi.nlm.nih.gov/pubmed/21520334
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.21508
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