Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2-Reference-Cited by-同舟云学术

Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2

Published:2013-10-26 Issue:6 Volume:23 Page:1538-1550
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Michalakis Stylianos,Shaltiel Lior,Sothilingam Vithiyanjali,Koch Susanne,Schludi Verena,Krause Stefanie,Zeitz Christina,Audo Isabelle,Lancelot Marie-Elise,Hamel Christian,Meunier Isabelle,Preising Markus N.,Friedburg Christoph,Lorenz Birgit,Zabouri Nawal,Haverkamp Silke,Garrido Marina Garcia,Tanimoto Naoyuki,Seeliger Mathias W.,Biel Martin,Wahl-Schott Christian A.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/23/6/1538/14142723/ddt541.pdf

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3. Functional characterization of the L-type Ca2+ channel Cav1.4alpha1 from mouse retina;Baumann;Invest Ophthalmol. Vis. Sci.,2004

4. Switching off calcium-dependent inactivation in L-type calcium channels by an autoinhibitory domain;Wahl-Schott;Proc. Natl Acad. Sci. USA,2006

5. The CACNA1F gene encodes an L-type calcium channel with unique biophysical properties and tissue distribution;McRory;J. Neurosci.,2004

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