Ion channels in health and disease-Reference-Cited by-同舟云学术

Ion channels in health and disease

Published:2001-07 Issue:7 Volume:2 Page:568-573
ISSN:1469-221X
Container-title:EMBO reports
language:en
Short-container-title:EMBO Rep

Author:

Niemeyer Barbara A¹,Mery Laurence²,Zawar Christian²,Suckow Arnt³,Monje Francisco³,Pardo Luis A³,Stühmer Walter³,Flockerzi Veit¹,Hoth Markus²

Affiliation:

1. Institut für Pharmakologie und Toxikologie Homburg Germany

2. Institut für Physiologie, Universität des Saarlandes Homburg Germany

3. Max‐Planck‐Institut für Experimentelle Medizin Göttingen Germany

Publisher

EMBO

Subject

Genetics,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1093/embo-reports/kve145

Reference26 articles.

1. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1

2. A novel sodium channel mutation in a family with hypokalemic periodic paralysis

3. Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1

4. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

5. Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X‐linked hereditary nephrolithiasis);Fisher S.E.;Hum. Mol. Genet.,1994

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