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Homozygous deletion of exon 18 leads to degradation of the lysosomal α-glucosidase precursor and to the infantile form of glycogen storage disease type II
Margreet G. E. M. Ausems, Marian A. Kroos, Magna Van der Kraan, Jan A. M. Smeitink, Wim J. Kleijer, Hans Kristian Ploos van Amstel, Arnold J. J. ReuserVolume:
49
Year:
1996
Language:
english
Pages:
4
DOI:
10.1111/j.1399-0004.1996.tb03801.x
File:
PDF, 488 KB
english, 1996