Publication | Closed Access
A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes
180
Citations
23
References
2003
Year
Novel MutationChannelopathiesMendelian DisorderBartter SyndromesChloride Channel GeneGeneticsGenetic DisorderPathologyMolecular GeneticsMedicine
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