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

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.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0013-0044-2 Version Permalink: http://hdl.handle.net/11858/00-001M-0000-002A-C5E1-F
Genre: Journal Article

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 Creators:
Derst, C., Author
Konrad, M., Author
Kockerling, A., Author
Karolyi, L., Author
Deschenes, G., Author
Daut, J., Author
Karschin, A.1, Author              
Seyberth, H. W., Author
Affiliations:
1Research Group of Molecular Neurobiology of Signal Transduction, MPI for biophysical chemistry, Max Planck Society, ou_578561              

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Language(s): eng - English
 Dates: 1997-01-23
 Publication Status: Published in print
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Method: Peer
 Identifiers: eDoc: 260944
ISI: 1997
 Degree: -

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Title: Biochemical and Biophysical Research Communications
  Alternative Title : Biochem. Biophys. Res. Commun.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 230 (3) Sequence Number: - Start / End Page: 641 - 645 Identifier: ISSN: 0006-291X