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TheADD1G460W polymorphism is not associated with variation in blood pressure in Canadian Oji-Cree

✍ Scribed by Christopher P. Busch; Stewart B. Harris; Anthony J. G. Hanley; Bernard Zinman; Robert A. Hegele


Book ID
106252525
Publisher
Nature Publishing Group
Year
1999
Tongue
English
Weight
67 KB
Volume
44
Category
Article
ISSN
1435-232X

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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