Your browser does not fully support modern features. Please upgrade for a smoother experience.
Submitted Successfully!
Thank you for your contribution! You can also upload a video entry or images related to this topic. For video creation, please contact our Academic Video Service.
Version Summary Created by Modification Content Size Created at Operation
1 Vicky Zhou + 464 word(s) 464 2020-12-15 07:47:53

Video Upload Options

We provide professional Academic Video Service to translate complex research into visually appealing presentations. Would you like to try it?
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Zhou, V. CLCNKA Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5147 (accessed on 22 September 2026).
Zhou V. CLCNKA Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5147. Accessed September 22, 2026.
Zhou, Vicky. "CLCNKA Gene" Encyclopedia, https://encyclopedia.pub/entry/5147 (accessed September 22, 2026).
Zhou, V. (2020, December 24). CLCNKA Gene. In Encyclopedia. https://encyclopedia.pub/entry/5147
Zhou, Vicky. "CLCNKA Gene." Encyclopedia. Web. 24 December, 2020.
CLCNKA Gene
Edit

chloride voltage-gated channel Ka

genes

References

  1. Barlassina C, Dal Fiume C, Lanzani C, Manunta P, Guffanti G, Ruello A, BianchiG, Del Vecchio L, Macciardi F, Cusi D. Common genetic variants and haplotypes in renal CLCNKA gene are associated to salt-sensitive hypertension. Hum Mol Genet.2007 Jul 1;16(13):1630-8.
  2. Kieferle S, Fong P, Bens M, Vandewalle A, Jentsch TJ. Two highly homologousmembers of the ClC chloride channel family in both rat and human kidney. ProcNatl Acad Sci U S A. 1994 Jul 19;91(15):6943-7.
  3. Krämer BK, Bergler T, Stoelcker B, Waldegger S. Mechanisms of Disease: thekidney-specific chloride channels ClCKA and ClCKB, the Barttin subunit, and theirclinical relevance. Nat Clin Pract Nephrol. 2008 Jan;4(1):38-46. Review.
  4. Nozu K, Inagaki T, Fu XJ, Nozu Y, Kaito H, Kanda K, Sekine T, Igarashi T,Nakanishi K, Yoshikawa N, Iijima K, Matsuo M. Molecular analysis of digenicinheritance in Bartter syndrome with sensorineural deafness. J Med Genet. 2008Mar;45(3):182-6. doi: 10.1136/jmg.2007.052944.
  5. Schlingmann KP, Konrad M, Jeck N, Waldegger P, Reinalter SC, Holder M,Seyberth HW, Waldegger S. Salt wasting and deafness resulting from mutations intwo chloride channels. N Engl J Med. 2004 Mar 25;350(13):1314-9.
More
Upload a video for this entry
Information
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Vicky Zhou
View Times: 698
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 24 Dec 2020
Notice
You are not a member of the advisory board for this topic. If you want to update advisory board member profile, please contact office@encyclopedia.pub.
OK
Confirm
Only members of the Encyclopedia advisory board for this topic are allowed to note entries. Would you like to become an advisory board member of the Encyclopedia?
Yes
No
${ textCharacter }/${ maxCharacter }
Submit
Cancel
There is no comment~
${ textCharacter }/${ maxCharacter }
Submit
Cancel
${ selectedItem.replyTextCharacter }/${ selectedItem.replyMaxCharacter }
Submit
Cancel
Confirm
Are you sure to Delete?
Yes No
Academic Video Service