Hepatocyte-specific glucose-6-phosphatase deficiency disturbs platelet aggregation and decreases blood monocytes upon fasting-induced hypoglycemia

Author:

La Rose Anouk M.,Bazioti VenetiaORCID,Hoogerland Joanne A.,Svendsen Arthur F.,Groenen Anouk G.ORCID,van Faassen Martijn,Rutten Martijn G.S.ORCID,Kloosterhuis Niels J.,Dethmers-Ausema Bertien,Nijland J. Hendrik,Mithieux Gilles,Rajas FabienneORCID,Kuipers Folkert,Lukens Michaël V.,Soehnlein Oliver,Oosterveer Maaike H.,Westerterp MaritORCID

Funder

Rijksuniversiteit Groningen

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology

Reference90 articles.

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2. Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type 1a;Lei;Science,1993

3. Genetic basis of glycogen storage disease type 1a: prevalent mutations at the glucose-6-phosphatase locus;Lei;The American Journal of Human Genetics,1995

4. Mutation analysis in 24 French patients with glycogen storage disease type la;Chevalier-Porst;Journal of Medical Genetics,1996

5. Recent development and gene therapy for glycogen storage disease type Ia;Chou;Liver Research,2017

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