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Mutations in the ROMK gene in antenatal Bartter syndrome are associated with impaired K+ channel function

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Karschin,  A.
Research Group of Molecular Neurobiology of Signal Transduction, MPI for biophysical chemistry, Max Planck Society;

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Derst, C., Konrad, M., Kockerling, A., Karolyi, L., Deschenes, G., Daut, J., et al. (1997). Mutations in the ROMK gene in antenatal Bartter syndrome are associated with impaired K+ channel function. Biochemical and Biophysical Research Communications, 230(3), 641-645.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0013-0044-2
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