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

Source:http://linkedlifedata.com/resource/pubmed/id/18003898

Proc. Natl. Acad. Sci. U.S.A. 2007 Nov 20 104 47 18537-42

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PMID
18003898