![](/img/cover-not-exists.png)
Development of a clinical assay for detection of GAA mutations and characterization of the GAA mutation spectrum in a Canadian cohort of individuals with glycogen storage disease, type II
M.E. McCready, N.L. Carson, P. Chakraborty, J.T.R. Clarke, J.W. Callahan, M.A. Skomorowski, A.K.J. Chan, F. Bamforth, R. Casey, C.A. Rupar, M.T. GeraghtyVolume:
92
Year:
2007
Language:
english
DOI:
10.1016/j.ymgme.2007.07.006
File:
PDF, 687 KB
english, 2007