A novel acid α-glucosidase mutation identified in a Pakistani family with glycogen storage disease type II

1997-09-04

Additional Metadata
Persistent URL	doi.org/10.1023/A:1005394706622, hdl.handle.net/1765/56231
Journal	Journal of Inherited Metabolic Disease
Organisation	Department of Clinical Genetics
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Kroos, M., Waitfield, A., Joosse, M., Winchester, B., Reuser, A., & MacDermot, K. (1997). A novel acid α-glucosidase mutation identified in a Pakistani family with glycogen storage disease type II. Journal of Inherited Metabolic Disease, 20(4), 556–558. doi:10.1023/A:1005394706622

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