An Ryr1^I4B95T mutation abolishes Ca²⁺ release channel function and delays development in homozygous offspring of a mutant mouse line.

Autor: Zvaritch, Elena, Depreux, Frederic, Kraeva, Natasha, Loy, Ryan E., Goonasekera, Sanjeewa A., Boncompagi, Simona, Kraev, Alexander, Gramolini, Anthony O., Dirksen, Robert T., Franzini-Armstrong, Clara, Seidman, Christine E., Seidman, J. G., MacLennan, David H.

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America; 11/20/2007, Vol. 104 Issue 47, p18537-18542, 6p, 3 Diagrams, 1 Graph