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References

These sources were used to develop the Genetics Home Reference gene summary on the AGL gene.

Cheng A, Zhang M, Okubo M, Omichi K, Saltiel AR. Distinct mutations in the glycogen debranching enzyme found in glycogen storage disease type III lead to impairment in diverse cellular functions. Hum Mol Genet. 2009 Jun 1;18(11):2045-52. doi: 10.1093/hmg/ddp128. Epub 2009 Mar 19. PubMed citation
Endo Y, Horinishi A, Vorgerd M, Aoyama Y, Ebara T, Murase T, Odawara M, Podskarbi T, Shin YS, Okubo M. Molecular analysis of the AGL gene: heterogeneity of mutations in patients with glycogen storage disease type III from Germany, Canada, Afghanistan, Iran, and Turkey. J Hum Genet. 2006;51(11):958-63. Epub 2006 Sep 19. PubMed citation
Entrez Gene
Frisbie JH, O'Connell DJ, Tow DE, Sasahara AA, Belko JS. Autologous radioiodinated fibrinogen, simplified. J Nucl Med. 1975 May;16(5):393-401. PubMed citation
Lucchiari S, Pagliarani S, Salani S, Filocamo M, Di Rocco M, Melis D, Rodolico C, Musumeci O, Toscano A, Bresolin N, Comi GP. Hepatic and neuromuscular forms of glycogenosis type III: nine mutations in AGL. Hum Mutat. 2006 Jun;27(6):600-1. PubMed citation
OMIM: AMYLO-1,6-GLUCOSIDASE, 4-ALPHA-GLUCANOTRANSFERASE

Reviewed: September 2010

Published: May 20, 2013