Add to ORKG[[sponsorship]]生物醫學科學研究所[[note]]已出版;[SCI];有審查制度;具代表性[[note]]http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=Drexel&SrcApp=hagerty_opac&KeyRecord=0964-6906&DestApp=JCR&RQ=IF_CAT_BOXPLOT[[note]]http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=RID&SrcApp=RID&DestLinkType=FullRecord&DestApp=ALL_WOS&KeyUT=00028600630000
[[sponsorship]]生物醫學科學研究所[[note]]已出版;[SCI];有審查制度;具代表性[[note]]http://gateway.isiknowledge.com/gateway/...
none7noAn abnormal structural form of glycogen (with less branching points or amylopectin-like polys...
Glycogen storage disease type III (GSD III) is partof a rare group of inherited enzyme defects that ...
Copyright © 2012 Tolga Aksu et al. This is an open access article distributed under the Creative Com...
g.oxfordjournals.org/ D ow nloaded from 2 Glycogen storage disease type IV (GSD-IV) is an autosomal ...
Glycogen storage disease type III (GSD III) is an autosomal recessive disease, due to deficiency of ...
We describe a new type of cardiomyopathy caused by a mutation in the glycogenin-1 gene (GYG1). Three...
We describe a new type of cardiomyopathy caused by a mutation in the glycogenin-1 gene (GYG1). Three...
[[sponsorship]]生物醫學科學研究所[[note]]已出版;[SCI];沒有審查制度;具代表性[[note]]http://gateway.isiknowledge.com/gateway...
Defects in enzymes involved in glycogen metabolism result in glycogen storage diseases (GSDs), which...
Purpose: To investigate the distribution and clinical impact of glycogen accumulation on heart struc...
International audienceGlycogen storage disorder type III (GSDIII) is a rare inborn error of metaboli...
[[sponsorship]]生物醫學科學研究所[[note]]已出版;[SCI];有審查制度;具代表性[[note]]http://gateway.isiknowledge.com/gateway/...
Glycogen branching enzyme deficiency (glycogen storage disease type IV, GSD-IV) is a rare autosomal ...
Glycogen synthesis is crucial for storing glucose residues that are released in case of energy deman...
[[sponsorship]]生物醫學科學研究所[[note]]已出版;[SCI];有審查制度;具代表性[[note]]http://gateway.isiknowledge.com/gateway/...
none7noAn abnormal structural form of glycogen (with less branching points or amylopectin-like polys...
Glycogen storage disease type III (GSD III) is partof a rare group of inherited enzyme defects that ...
Copyright © 2012 Tolga Aksu et al. This is an open access article distributed under the Creative Com...
g.oxfordjournals.org/ D ow nloaded from 2 Glycogen storage disease type IV (GSD-IV) is an autosomal ...
Glycogen storage disease type III (GSD III) is an autosomal recessive disease, due to deficiency of ...
We describe a new type of cardiomyopathy caused by a mutation in the glycogenin-1 gene (GYG1). Three...
We describe a new type of cardiomyopathy caused by a mutation in the glycogenin-1 gene (GYG1). Three...
[[sponsorship]]生物醫學科學研究所[[note]]已出版;[SCI];沒有審查制度;具代表性[[note]]http://gateway.isiknowledge.com/gateway...
Defects in enzymes involved in glycogen metabolism result in glycogen storage diseases (GSDs), which...
Purpose: To investigate the distribution and clinical impact of glycogen accumulation on heart struc...
International audienceGlycogen storage disorder type III (GSDIII) is a rare inborn error of metaboli...
[[sponsorship]]生物醫學科學研究所[[note]]已出版;[SCI];有審查制度;具代表性[[note]]http://gateway.isiknowledge.com/gateway/...
Glycogen branching enzyme deficiency (glycogen storage disease type IV, GSD-IV) is a rare autosomal ...
Glycogen synthesis is crucial for storing glucose residues that are released in case of energy deman...
[[sponsorship]]生物醫學科學研究所[[note]]已出版;[SCI];有審查制度;具代表性[[note]]http://gateway.isiknowledge.com/gateway/...
none7noAn abnormal structural form of glycogen (with less branching points or amylopectin-like polys...
Glycogen storage disease type III (GSD III) is partof a rare group of inherited enzyme defects that ...