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An Ryr1I4895T mutation abolishes Ca2+ release channel function and delays development in homozygous offspring of a mutant mouse line

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Description scientific journal article
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author: Natasha Kraeva  Elena Zvaritch  Alexander Kraev  Jonathan G Seidman  Clara Franzini-Armstrong  Christine E. Seidman  Frederic F S Depreux 

Publication date November 20, 2007
Language English
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