Author:
Douillard-Guilloux Gaelle,Raben Nina,Takikita Shoichi,Ferry Arnaud,Vignaud Alban,Guillet-Deniau Isabelle,Favier Maryline,Thurberg Beth L.,Roach Peter J.,Caillaud Catherine,Richard Emmanuel
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Reference45 articles.
1. Glycogen storage disease type II: acid alpha-glucosidase (acid maltase) deficiency;Hirschhorn,2001
2. Pompe disease diagnosis and management guideline;Kishnani;Genet. Med.,2006
3. Glycogen storage disease type II: birth prevalence agrees with predicted genotype frequency;Ausems;Community Genet.,1999
4. Targeted disruption of the acid alpha-glucosidase gene in mice causes an illness with critical features of both infantile and adult human glycogen storage disease type II;Raben;J. Biol. Chem.,1998
5. Generalized glycogen storage and cardiomegaly in a knockout mouse model of Pompe disease;Bijvoet;Hum. Mol. Genet.,1998
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