Preferred Label : glycogen phosphorylase, liver form;

MeSH definition : An isoenzyme of GLYCOGEN PHOSPHORYLASE that catalyzes the degradation of GLYCOGEN in liver tissue. Mutation of the gene coding this enzyme on chromosome 14 is the cause of GLYCOGEN STORAGE DISEASE TYPE VI.;

MeSH hyponym : glycogen phosphorylase a, liver form; glycogen phosphorylase b, liver form;

MeSH Related Number : glycogen phosphorylase b, liver form; glycogen phosphorylase a, liver form;

Registry Number MeSH : EC 2.4.1.-;

Related CAS MeSH : EC 2.4.1.- (Glycogen phosphorylase b, liver form); EC 2.4.1.- (Glycogen phosphorylase a, liver form);

Is substance : O;

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An isoenzyme of GLYCOGEN PHOSPHORYLASE that catalyzes the degradation of GLYCOGEN in liver tissue. Mutation of the gene coding this enzyme on chromosome 14 is the cause of GLYCOGEN STORAGE DISEASE TYPE VI.

http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=369
2009
true
France
French
glycogen phosphorylase, liver form
glycogen storage disease type vi
scientific and technical information

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27/07/2025


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