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The Journal of Clinical Endocrinology and Metabolism|July 11, 2002
Novel mutations responsible for autosomal recessive multisystem pseudohypoaldosteronism and sequence variants in epithelial sodium channel alpha-, beta-, and gamma-subunit genesAnjana Saxena, Israel Hanukoglu, Deepak Saxena, et al.Clinical Endocrinology|April 28, 2005
Novel mutations in epithelial sodium channel (ENaC) subunit genes and phenotypic expression of multisystem pseudohypoaldosteronismOded Edelheit, Israel Hanukoglu, Maria Gizewska, et al.Gene|May 7, 2016
Gene Wiki Reviews-Raising the quality and accessibility of information about the human genomeGinger Tsueng, Benjamin M Good, Peipei Ping, et al.Human Genetics|December 25, 2010
Autosomal recessive hyponatremia due to isolated salt wasting in sweat associated with a mutation in the active site of Carbonic Anhydrase 12Emad Muhammad, Neta Leventhal, Galit Parvari, et al.British Journal of Pharmacology|September 16, 2021
THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: Ion channelsStephen Ph Alexander, Alistair Mathie, John A Peters, et al.British Journal of Pharmacology|December 20, 2023
The Concise Guide to PHARMACOLOGY 2023/24: Ion channelsStephen P H Alexander, Alistair A Mathie, John A Peters, et al.British Journal of Pharmacology|December 29, 2025
The Concise Guide to PHARMACOLOGY 2025/26: Ion channelsStephen P H Alexander, Jörg Striessnig, Alasdair J Gibb, et al.Pageof 3