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. Author manuscript; available in PMC: 2013 Feb 28.
Published in final edited form as: Pflugers Arch. 2008 Nov 4;458(1):61–76. doi: 10.1007/s00424-008-0607-1

Fig. 3.

Fig. 3

Missense mutations informed for NKCC2. Mutations in blue were informed as harbored by patients with Bartter syndrome [2, 12, 51, 92, 136, 137, 148]. Mutations in red were informed in normal subjects of the Framingham Heart Study [85]