HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K+/Cl− co-transporter 3-Reference-Cited by-同舟云学术

HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K+/Cl− co-transporter 3

Published:2008-06-19 Issue:17 Volume:17 Page:2703-2711
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Salin-Cantegrel Adèle,Shekarabi Masoud,Holbert Sébastien,Dion Patrick,Rochefort Daniel,Laganière Janet,Dacal Sandra,Hince Pascale,Karemera Liliane,Gaspar Claudia,Lapointe Jean-Yves,Rouleau Guy A.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/17/17/2703/17245377/ddn172.pdf

Reference37 articles.

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2. The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum;Howard;Nat. Genet.,2002

3. Cloning and characterization of KCC3 and KCC4, new members of the cation-chloride cotransporter gene family;Mount;J. Biol. Chem.,1999

4. Molecular physiology of cation-coupled Cl− cotransport: the SLC12 family;Hebert;Pflugers Arch.,2004

5. Cloning, characterization, and chromosomal location of a novel human K+-Cl− cotransporter;Hiki;J. Biol. Chem.,1999

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