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Autor:
Kockskämper, Hauke Fender, Kim Walter, Aytug K. Kiper, Jelena Plačkić, Theresa M. Kisko, Moria D. Braun, Rainer K. W. Schwarting, Susanne Rohrbach, Markus Wöhr, Niels Decher, Jens
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 12; Pages: 9795
CACNA1C encodes the pore-forming α1C subunit of the L-type Ca2+ channel, Cav1.2. Mutations and polymorphisms of the gene are associated with neuropsychiatric and cardiac disease. Haploinsufficient Cacna1c+/− rats represent a recently developed mod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::0273897fa27149038c8f7ab55c35a751
