Loss of Cav1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness-Reference-Cited by-同舟云学术

Loss of Cav1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness

Published:2010-12-05 Issue:1 Volume:14 Page:77-84
ISSN:1097-6256
Container-title:Nature Neuroscience
language:en
Short-container-title:Nat Neurosci

Author:

Baig Shahid M,Koschak Alexandra,Lieb Andreas,Gebhart Mathias,Dafinger Claudia,Nürnberg Gudrun,Ali Amjad,Ahmad Ilyas,Sinnegger-Brauns Martina J,Brandt Niels,Engel Jutta,Mangoni Matteo E,Farooq Muhammad,Khan Habib U,Nürnberg Peter,Striessnig Jörg,Bolz Hanno J

Publisher

Springer Science and Business Media LLC

Subject

General Neuroscience

Link

http://www.nature.com/articles/nn.2694.pdf

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4. Dou, H. et al. Null mutation of alpha1D Ca2+ channel gene results in deafness but no vestibular defect in mice. J. Assoc. Res. Otolaryngol. 5, 215–226 (2004).

5. Platzer, J. et al. Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels. Cell 102, 89–97 (2000).

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