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About this Medicine article
Novel NCCT Gene Mutations as a Cause of Gitelman’s Syndrome and a Systematic Review of Mutant and Polymorphic NCCT Alleles by Reissinger, Annette; Ludwig, Michael; Utsch, Boris; Prömse, Astrid; Baulmann, Johannes; Weisser, Burkhard; Vetter, Hans; Kramer, Herbert J.; Bokemeyer, Dirk is a Medicine article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Medicine.
- Author
- Reissinger, Annette; Ludwig, Michael; Utsch, Boris; Prömse, Astrid; Baulmann, Johannes; Weisser, Burkhard; Vetter, Hans; Kramer, Herbert J.; Bokemeyer, Dirk
- Publisher
- S. Karger AG (ISSN 1420-4096)
- Published
- 2003
- Language
- EN
- Field
- Medicine (Health Sciences)