Novel polymorphic AluYb8 insertion in th
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Margus Putku; Katrin Kepp; Elin Org; Siim SΓ΅ber; David Comas; Margus Viigimaa; G
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Article
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2011
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John Wiley and Sons
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English
β 221 KB
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