Novel NCCT Gene Mutations as a Cause of Gitelman’s Syndrome and a Systematic Review of Mutant and Polymorphic NCCT Alleles

Publisher： Karger

E-ISSN： 1423-0143|25|6|354-362

ISSN： 1420-4096

Source： Kidney and Blood Pressure Research, Vol.25, Iss.6, 2003-02, pp. : 354-362

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