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Dive into the research topics of 'Loss of Ca v 1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness'. Together they form a unique fingerprint.- Sort by
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Shahid M. Baig, Alexandra Koschak, Andreas Lieb, Mathias Gebhart, Claudia Dafinger, Gudrun Nürnberg, Amjad Ali, Ilyas Ahmad, Martina J. Sinnegger-Brauns, Niels Brandt, Jutta Engel, Matteo E. Mangoni, Muhammad Farooq, Habib U. Khan, Peter Nürnberg, Jörg Striessnig, Hanno J. Bolz